Canonical Allele Identifier: PA2826626721
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1784361
ClinVar RCV Id: RCV002417298
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly540Arg
CA009551
NM_001281492.2:c.1618G>A
CA346750677
NM_001281492.2:c.1618G>C