Canonical Allele Identifier: PA2579923507
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3230840
ClinVar RCV Id: RCV004522954

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln879Glu
CA346731314
NM_000251.3:c.2635C>G