Canonical Allele Identifier: PA2825076062
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2017167
ClinVar RCV Id: RCV002835064
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu902del
CA2580611305
NM_000251.3:c.2704_2706del