Allele Registry

Canonical Allele Identifier: PA229683

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089028

RCV001261644

ClinVar Variation:

102777

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ile224Thr	CA229682 NM_000277.3:c.671T>C