Canonical Allele Identifier: PA916012012
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89409
ClinVar Variation Id: 578919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp879Glu
CA013331
NM_001281494.2:c.2637C>G
CA346760250
NM_001281494.2:c.2637C>A