Canonical Allele Identifier: PA165317
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141396

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu851Val
CA020713
NM_000251.3:c.2551C>G