Canonical Allele Identifier: PA197859
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 187518
ClinVar RCV Id: RCV000167253 RCV000490613 RCV000817438 RCV001270946
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Cys697Tyr
CA019995
NM_000251.3:c.2090G>A