Canonical Allele Identifier: PA2573168918
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1354193
ClinVar RCV Id: RCV001887747

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Cys244Gly
CA382035232
NM_000372.5:c.730T>G