Canonical Allele Identifier: PA658680600
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455137
ClinVar RCV Id: RCV000540859 RCV000583949
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Tyr478Cys
CA346745524
NM_000179.3:c.1433A>G