Canonical Allele Identifier: PA229712
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102800
ClinVar RCV Id: RCV000089051 RCV001215843
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly239Val
CA229711
NM_000277.3:c.716G>T