Canonical Allele Identifier: PA2826625893
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1772651
ClinVar RCV Id: RCV002394307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val350Ile
CA346745593
NM_001281492.2:c.1048G>A