Canonical Allele Identifier: PA2826631091
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444000
ClinVar RCV Id: RCV001981571

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu373Gln
CA346750704
NM_001281493.2:c.1117G>C