Canonical Allele Identifier: PA2826633246
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 823881
ClinVar RCV Id: RCV001020518
ClinVar Variation Id: 1347029
ClinVar RCV Id: RCV002032950

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Phe872Leu
CA346760210
NM_001281493.2:c.2614T>C
CA346760215
NM_001281493.2:c.2616T>A
CA346760216
NM_001281493.2:c.2616T>G