Canonical Allele Identifier: PA2826586987
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525848
ClinVar RCV Id: RCV000630193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ile1011_Gln1012insHisIle
CA658795758
NM_001281494.2:c.3030_3035dup