Canonical Allele Identifier: PA1139677303
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 959916
ClinVar RCV Id: RCV001233350

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu226Gly
CA346731826
NM_000251.3:c.677A>G