Canonical Allele Identifier: PA2826625733
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185673

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asp309Gly
CA008484
NM_001281492.2:c.926A>G