Canonical Allele Identifier: PA2826634306
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184803

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr25Ser
CA016745
NM_001281494.2:c.74C>G
CA346741015
NM_001281494.2:c.73A>T