Canonical Allele Identifier: PA645475851
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246167

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln846_Lys847del
CA10584224
NM_000251.3:c.2536_2541del