Canonical Allele Identifier: PA2826463158
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1755571
ClinVar RCV Id: RCV002369539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg161Lys
CA346731845
NM_001258281.1:c.482G>A