Allele Registry

Canonical Allele Identifier: PA105946

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088865

RCV000758100

ClinVar Variation:

102623

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ile65Asn	CA229479 NM_000277.3:c.194T>A