Canonical Allele Identifier: PA2580113769
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 2137231
ClinVar RCV Id: RCV003062446
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Ala241Thr
CA6221178
NM_000372.5:c.721G>A