Canonical Allele Identifier: PA2826627499
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 135836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys724Ile
CA010405
NM_001281492.2:c.2171_2172delinsTT