Canonical Allele Identifier: PA2573168990
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1500300
ClinVar RCV Id: RCV002015538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Asp448Gly
CA6221410
NM_000372.5:c.1343A>G