Canonical Allele Identifier: PA891846068
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 577305
ClinVar RCV Id: RCV000700018 RCV002360792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asp222Val
CA346739386
NM_000179.3:c.665A>T