Allele Registry

Canonical Allele Identifier: PA2825138166

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001199977

ClinVar Variation:

932253

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Leu348Pro	CA16020922 NM_000277.3:c.1043T>C