Canonical Allele Identifier: PA2826631618
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu496Val
CA010176
NM_001281493.2:c.1486C>G