Canonical Allele Identifier: PA2826465958
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135860
ClinVar RCV Id: RCV000122988 RCV000412095 RCV001558333 RCV002251992 RCV000573859 RCV003997408 RCV004542928
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile840Thr
CA020898
NM_001258281.1:c.2519T>C