Allele Registry

Canonical Allele Identifier: PA105416

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000000648

RCV000088815

RCV000401074

RCV003415609

ClinVar Variation:

617

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Asp415Asn	CA114364 NM_000277.3:c.1243G>A