Canonical Allele Identifier: PA2826624913
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 197114
ClinVar RCV Id: RCV000178052 RCV000215538 RCV000226497 RCV003996572
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg118Gly
CA016385
NM_001281492.2:c.352C>G