Canonical Allele Identifier: PA2826464941
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1783376
ClinVar RCV Id: RCV002421685

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asn587Lys
CA346728785
NM_001258281.1:c.1761T>A
CA346728787
NM_001258281.1:c.1761T>G