Canonical Allele Identifier: PA277202
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 212524
ClinVar RCV Id: RCV000193793
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Glu221Lys
CA277201
NM_000372.5:c.661G>A