Canonical Allele Identifier: PA891846073
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 568938
ClinVar RCV Id: RCV000689445 RCV000777461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly273Ala
CA346740411
NM_000179.3:c.818G>C