Canonical Allele Identifier: PA2826627213
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.His655Gln
CA16611005
NM_001281492.2:c.1965T>A
CA346753563
NM_001281492.2:c.1965T>G