Canonical Allele Identifier: PA2826627267
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790571
ClinVar RCV Id: RCV002430646
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu668del
CA2580067843
NM_001281492.2:c.2002_2004del