Allele Registry

Canonical Allele Identifier: PA916037654

Gene: PAH HGNC NCBI

ClinVar Allele:

15642

ClinVar RCV:

RCV000000634

RCV000078531

ClinVar Variation:

603

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Tyr277Asp	CA251534 NM_001354304.2:c.829T>G