Canonical Allele Identifier: PA2573168902
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1369550
ClinVar RCV Id: RCV001870690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Gln220Arg
CA382035071
NM_000372.5:c.659A>G