Allele Registry

Canonical Allele Identifier: PA2825138250

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001789809

ClinVar Variation:

1327547

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Asp415Tyr	CA16020978 NM_000277.3:c.1243G>T