Allele Registry

Canonical Allele Identifier: PA104902

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089160

RCV000668228

ClinVar Variation:

102897

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ala309Asp	CA229853 NM_000277.3:c.926C>A