Allele Registry

Canonical Allele Identifier: PA229850

Gene: PAH HGNC NCBI

ClinVar Allele:

108631

ClinVar RCV:

RCV000089158

ClinVar Variation:

102895

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Leu308Val	CA229849 NM_000277.3:c.922C>G