Canonical Allele Identifier: PA2826634267
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 485866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu16Lys
CA346740840
NM_001281494.2:c.46G>A