Allele Registry

Canonical Allele Identifier: PA1139728207

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001200005

ClinVar Variation:

932270

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Asn438Asp	CA16020992 NM_001354304.2:c.1312A>G