Canonical Allele Identifier: PA891846078
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 580321
ClinVar RCV Id: RCV000703816 RCV001018376 RCV002259365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Val294Gly
CA346740669
NM_000179.3:c.881T>G