Allele Registry

Canonical Allele Identifier: PA2825138143

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001789822

ClinVar Variation:

1327560

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Trp326Ser	CA16020913 NM_000277.3:c.977G>C