Canonical Allele Identifier: PA2826464624
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1057500
ClinVar RCV Id: RCV001366493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu514Lys
CA346728196
NM_001258281.1:c.1540G>A