Canonical Allele Identifier: PA2826634356
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1773547
ClinVar RCV Id: RCV002397121

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu45Lys
CA346741455
NM_001281494.2:c.133G>A