Allele Registry

Canonical Allele Identifier: PA2825138094

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001814820

ClinVar Variation:

1334639

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Pro281His	CA386294527 NM_000277.3:c.842C>A