Canonical Allele Identifier: PA2580113757
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 2130645
ClinVar RCV Id: RCV003044632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Pro152Arg
CA382034438
NM_000372.5:c.455C>G