Canonical Allele Identifier: PA2826628737
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1060721

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala1090Val
CA346760831
NM_001281492.2:c.3269C>T