Allele Registry

Canonical Allele Identifier: PA105974

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088864

RCV000803656

ClinVar Variation:

102622

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ile65Val	CA229478 NM_000277.3:c.193A>G