Allele Registry

Canonical Allele Identifier: PA2825137864

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001093427

ClinVar Variation:

872776

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ala49Asp	CA386302329 NM_000277.3:c.146C>A