Canonical Allele Identifier: PA100518
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 3776

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Arg77Gln
CA227543
NM_000372.5:c.230G>A