Canonical Allele Identifier: PA330444
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Leu798Val
CA010176
NM_000179.3:c.2392C>G