Allele Registry

Canonical Allele Identifier: PA2825138272

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001789812

ClinVar Variation:

1327550

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ala434Val	CA16020990 NM_000277.3:c.1301C>T