Canonical Allele Identifier: PA2826464625
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1779135
ClinVar RCV Id: RCV002399288

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu514Ala
CA346728198
NM_001258281.1:c.1541A>C