Allele Registry

Canonical Allele Identifier: PA105216

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000000607

RCV000078507

RCV002287314

RCV002512607

RCV003415607

ClinVar Variation:

577

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Arg408Trp	CA251523 NM_000277.3:c.1222C>T