Canonical Allele Identifier: PA2825138126
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 1458264
ClinVar RCV Id: RCV001972839

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly312Val
CA16020902
NM_000277.3:c.935G>T