HP c.111C>A ;(p.P37=)

Variant ID: 16-72090451-C-A

NM_005143.3(HP):c.111C>A;(p.P37=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Mutations of human cationic trypsinogen (PRSS1) and chronic pancreatitis.

Human Mutation
Teich, Niels N; Rosendahl, Jonas J; Tóth, Miklós M; Mössner, Joachim J; Sahin-Tóth, Miklós M
Publication Date: 2006-08

Variant appearance in text: HP: 111C>A
PubMed Link: 16791840
Variant Present in the following documents:
  • Main text
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