Canonical Allele Identifier: PA100892
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 99560
ClinVar RCV Id: RCV000085943
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Gly97Arg
CA227556
NM_000372.5:c.289G>A
CA382034073
NM_000372.5:c.289G>C