Canonical Allele Identifier: PA2826625144
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 822941
ClinVar RCV Id: RCV001018720

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg172Gly
CA346740708
NM_001281492.2:c.514A>G