Canonical Allele Identifier: PA2573168831
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1354013
ClinVar RCV Id: RCV001874000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Ile123Thr
CA382034245
NM_000372.5:c.368T>C