Canonical Allele Identifier: PA2826627264
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu668Val
CA010176
NM_001281492.2:c.2002C>G