Canonical Allele Identifier: PA2826627106
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 140836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg631Gly
CA009950
NM_001281492.2:c.1891A>G