Allele Registry

Canonical Allele Identifier: PA2825138128

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001970975

ClinVar Variation:

1474010

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Asp315Glu	CA386291635 NM_000277.3:c.945T>G CA386291637 NM_000277.3:c.945T>A