Allele Registry

Canonical Allele Identifier: PA105182

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089106

RCV003323400

ClinVar Variation:

102847

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Arg270Ser	CA229782 NM_000277.3:c.810A>T CA386294571 NM_000277.3:c.810A>C