Canonical Allele Identifier: PA2826627664
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1794632
ClinVar RCV Id: RCV002428866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu763Arg
CA346755275
NM_001281492.2:c.2288T>G