Canonical Allele Identifier: PA193999
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 186151
ClinVar RCV Id: RCV000165690 RCV000202197 RCV000766654 RCV000798203 RCV003462184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile766Val
CA020456
NM_000251.3:c.2296A>G