Allele Registry

Canonical Allele Identifier: PA104921

Gene: PAH HGNC NCBI

ClinVar Allele:

15655

ClinVar RCV:

RCV000000647

RCV000089177

RCV000675108

RCV002251845

ClinVar Variation:

616

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ala322Gly	CA114363 NM_000277.3:c.965C>G