Canonical Allele Identifier: PA2826627628
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89306
ClinVar RCV Id: RCV001016227 RCV001854278
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile756Val
CA010670
NM_001281492.2:c.2266A>G