Allele Registry

Canonical Allele Identifier: PA916037608

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089084

ClinVar Variation:

102827

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Gly257Ser	CA229748 NM_001354304.2:c.769G>A