Canonical Allele Identifier: PA229326
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102512
ClinVar RCV Id: RCV000088743 RCV001543652
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Tyr356His
CA229325
NM_000277.3:c.1066T>C