Canonical Allele Identifier: PA2826627113
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1789060
ClinVar RCV Id: RCV002446208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asp633Glu
CA346752948
NM_001281492.2:c.1899T>A
CA346752954
NM_001281492.2:c.1899T>G