Canonical Allele Identifier: PA2826625277
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1768750
ClinVar RCV Id: RCV002382967

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu202Asp
CA346741137
NM_001281492.2:c.606A>T
CA346741142
NM_001281492.2:c.606A>C