Canonical Allele Identifier: PA2826629208
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1736284
ClinVar RCV Id: RCV002357563
ClinVar Variation Id: 2819276
ClinVar RCV Id: RCV003760967

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu1181Asp
CA072317
NM_001281492.2:c.3543A>C
CA346761486
NM_001281492.2:c.3543A>T