Allele Registry

Canonical Allele Identifier: PA916037454

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088932

RCV001093515

ClinVar Variation:

102684

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Tyr154Asn	CA229556 NM_001354304.2:c.460T>A