Allele Registry

Canonical Allele Identifier: PA2825138275

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001200005

ClinVar Variation:

932270

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Asn438Asp	CA16020992 NM_000277.3:c.1312A>G