Canonical Allele Identifier: PA2826633971
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 845670
ClinVar RCV Id: RCV001048782 RCV002374893
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg1016Gly
CA346761525
NM_001281493.2:c.3046A>G