Allele Registry

Canonical Allele Identifier: PA106832

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089064

RCV000632879

ClinVar Variation:

102811

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Val245Glu	CA229725 NM_000277.3:c.734T>A