Canonical Allele Identifier: PA2826627254
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790512
ClinVar RCV Id: RCV002459528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu666del
CA2580611373
NM_001281492.2:c.1998_2000del