Canonical Allele Identifier: PA100711
Gene: TYR HGNC NCBI

Linked Data

ClinVar Variation Id: 39977
ClinVar RCV Id: RCV000033111 RCV002513316 RCV003466887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000363.1:p.Cys91Tyr
CA261236
NM_000372.5:c.272G>A