Canonical Allele Identifier: PA2573168804
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 1366846
ClinVar RCV Id: RCV001962164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Val83Ile
CA6221069
NM_000372.5:c.247G>A