Canonical Allele Identifier: PA2826628628
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 927298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu1066Val
CA346760527
NM_001281492.2:c.3197A>T