Canonical Allele Identifier: PA2826463226
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2808404
ClinVar RCV Id: RCV003760766

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg177Pro
CA346732181
NM_001258281.1:c.530G>C