Canonical Allele Identifier: PA2579912827
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2808404
ClinVar RCV Id: RCV003760766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg243Pro
CA346732181
NM_000251.3:c.728G>C