Allele Registry

Canonical Allele Identifier: PA229425

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088822

RCV000993606

ClinVar Variation:

102584

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Leu424Ser	CA229424 NM_000277.3:c.1271T>C