Canonical Allele Identifier: PA2573168901
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1501231
ClinVar RCV Id: RCV002017313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Glu219Ala
CA382035064
NM_000372.5:c.656A>C