Canonical Allele Identifier: PA645474221
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408522
ClinVar RCV Id: RCV000458164 RCV001143790 RCV003129864 RCV004022694
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala398Val
CA16610785
NM_000251.3:c.1193C>T