Canonical Allele Identifier: PA2826465645
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 663240
ClinVar RCV Id: RCV000821083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ala765Pro
CA346730641
NM_001258281.1:c.2293G>C