Canonical Allele Identifier: PA2826627539
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 859835
ClinVar RCV Id: RCV001066036 RCV002451284 RCV003886478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly734Arg
CA346754849
NM_001281492.2:c.2200G>C
CA346754859
NM_001281492.2:c.2200G>A