PAH c.981T>A ;(p.F327L)

Variant ID: 12-103238198-A-T

NM_000277.1(PAH):c.981T>A;(p.F327L)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Predicted effects of missense mutations on native-state stability account for phenotypic outcome in phenylketonuria, a paradigm of misfolding diseases.

American Journal Of Human Genetics
Pey, Angel L AL; Stricher, Francois F; Serrano, Luis L; Martinez, Aurora A
Publication Date: 2007-11

Variant appearance in text: PAH: F327L
PubMed Link: 17924342
Variant Present in the following documents:
  • Main text
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