Canonical Allele Identifier: PA2826636043
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 219956

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu472Val
CA348302
NM_001281494.2:c.1414C>G