Canonical Allele Identifier: PA105709
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102467
ClinVar RCV Id: RCV000088698 RCV001543648
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly337Val
CA229268
NM_000277.3:c.1010G>T