Canonical Allele Identifier: PA645475838
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 428459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.His829Gln
CA46707640
NM_000251.3:c.2487T>G
CA346730629
NM_000251.3:c.2487T>A