Canonical Allele Identifier: PA2826629245
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 861653
ClinVar RCV Id: RCV002355092 RCV001068220
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg1188Lys
CA46719858
NM_001281492.2:c.3563G>A