Canonical Allele Identifier: PA100698
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 3781
ClinVar RCV Id: RCV000003984 RCV000085941 RCV000626678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Cys89Arg
CA227553
NM_000372.5:c.265T>C