Allele Registry

Canonical Allele Identifier: PA229555

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088931

ClinVar Variation:

102683

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Asp151Gly	CA229554 NM_000277.3:c.452A>G