Canonical Allele Identifier: PA294457
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp487Glu
CA018356
NM_000251.3:c.1461C>G
CA346727006
NM_000251.3:c.1461C>A