Allele Registry

Canonical Allele Identifier: PA106660

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088932

RCV001093515

ClinVar Variation:

102684

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Tyr154Asn	CA229556 NM_000277.3:c.460T>A