Canonical Allele Identifier: PA160881
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 134845
ClinVar RCV Id: RCV000121565 RCV000820212 RCV002221491 RCV002426668 RCV003997349
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu849Val
CA020700
NM_000251.3:c.2545C>G