Canonical Allele Identifier: PA2825089459
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1789389
ClinVar RCV Id: RCV002446405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gly770Ser
CA346753103
NM_000179.3:c.2308G>A