Canonical Allele Identifier: PA229558
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102685
ClinVar RCV Id: RCV000088933 RCV001093509
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr154His
CA229557
NM_000277.3:c.460T>C