Allele Registry

Canonical Allele Identifier: PA2825138119

Gene: PAH HGNC NCBI

ClinVar Allele:

1318171

ClinVar RCV:

RCV001789829

ClinVar Variation:

1327567

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ala309Thr	CA16021003 NM_000277.3:c.925G>A