Allele Registry

Canonical Allele Identifier: PA2825138126

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001972839

ClinVar Variation:

1458264

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Gly312Val	CA16020902 NM_000277.3:c.935G>T