Canonical Allele Identifier: PA2826627121
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455186

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Cys635Ser
CA346752969
NM_001281492.2:c.1903T>A
CA346752975
NM_001281492.2:c.1904G>C