Canonical Allele Identifier: PA2826631447
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1788889

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu458Lys
CA346752868
NM_001281493.2:c.1372G>A