Canonical Allele Identifier: PA2826631038
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 629613
ClinVar RCV Id: RCV000774323 RCV001042028
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Thr361Ile
CA346750644
NM_001281493.2:c.1082C>T