Canonical Allele Identifier: PA165339
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141406
ClinVar RCV Id: RCV000129911 RCV000465942 RCV001551502 RCV003460906 RCV003997535
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser233Cys
CA022041
NM_000251.3:c.698C>G