Allele Registry

Canonical Allele Identifier: PA916037609

Gene: PAH HGNC NCBI

ClinVar Allele:

108566

ClinVar RCV:

RCV000089087

RCV000668413

ClinVar Variation:

102830

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Gly257Val	CA229753 NM_001354304.2:c.770G>T