Allele Registry

Canonical Allele Identifier: PA105101

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089054

RCV000153635

ClinVar Variation:

102803

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Arg241Cys	CA273357 NM_000277.3:c.721C>T