Canonical Allele Identifier: PA2826631513
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 219956

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Leu472Val
CA348302
NM_001281493.2:c.1414C>G