Canonical Allele Identifier: PA2826635906
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1788028
ClinVar RCV Id: RCV002428173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Leu441Trp
CA346752486
NM_001281494.2:c.1322T>G