Canonical Allele Identifier: PA2741816435
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 3028902
ClinVar RCV Id: RCV003890766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Trp80Cys
CA382033878
NM_000372.5:c.240G>C
CA382033880
NM_000372.5:c.240G>T