Canonical Allele Identifier: PA2826631226
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Glu405Gly
CA346750986
NM_001281493.2:c.1214A>G