Allele Registry

Canonical Allele Identifier: PA229392

Gene: PAH HGNC NCBI

ClinVar Allele:

108298

ClinVar RCV:

RCV000088796

RCV001543634

ClinVar Variation:

102562

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Arg400Thr	CA229391 NM_000277.3:c.1199G>C