Canonical Allele Identifier: PA2826627639
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 182637
ClinVar RCV Id: RCV000160683 RCV000205971 RCV000759138 RCV000781587 RCV001142302 RCV003462094 RCV003998497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys758Asn
CA010696
NM_001281492.2:c.2274G>C
CA346755217
NM_001281492.2:c.2274G>T