Canonical Allele Identifier: PA2826631412
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 924360
ClinVar Variation Id: 2701756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly450Ser
CA346752701
NM_001281493.2:c.1348G>A
CA2697548118
NM_001281493.2:c.1347_1348delinsCA