Canonical Allele Identifier: PA2826634010
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 957659
ClinVar RCV Id: RCV001230674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu1022Lys
CA346761559
NM_001281493.2:c.3064G>A