MLH1 c.2152_2153inv ;(p.H718C)

Variant ID: 3-37092025-CA-TG

NM_000249.3(MLH1):c.2152_2153inv;(p.H718C)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Lynch syndrome in a predominantly Afrocentric population: a clinicopathological and genetic study.

Canadian Journal Of Surgery. Journal Canadien De Chirurgie
Plummer, Joseph M JM; Chin, Sheray N SN; Aronson, Melyssa M; Graham, Rondell P RP; Williams, Nadia P NP; Bapat, Bharati B; Wharfe, Gillian G; Pollett, Aaron A; Gallinger, Steven S
Publication Date: 2012-10

Variant appearance in text: MLH1: His718Cys
PubMed Link: 22854115
Variant Present in the following documents:
  • Main text
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