Canonical Allele Identifier: PA2826627700
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1391382
ClinVar RCV Id: RCV001893047
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly770Asp
CA346755317
NM_001281492.2:c.2309G>A