Canonical Allele Identifier: PA2826627359
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 821309
ClinVar RCV Id: RCV001015602
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg690Gly
CA346754084
NM_001281492.2:c.2068A>G