Canonical Allele Identifier: PA2580113772
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1975949

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.His256Arg
CA382035405
NM_000372.5:c.767A>G