Canonical Allele Identifier: PA2826635667
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 489977
ClinVar RCV Id: RCV000580109 RCV000781578 RCV001346046
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly383Arg
CA346750763
NM_001281494.2:c.1147G>C