Allele Registry

Canonical Allele Identifier: PA105951

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088866

ClinVar Variation:

102624

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ile65Ser	CA229480 NM_000277.3:c.194T>G