Canonical Allele Identifier: PA2580113763
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1933203
ClinVar RCV Id: RCV002635860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Ile194Val
CA382034780
NM_000372.5:c.580A>G