Canonical Allele Identifier: PA658739819
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 489942
ClinVar RCV Id: RCV000580301 RCV000629841 RCV001193286 RCV002245022 RCV004001259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile883Met
CA037199
NM_000251.3:c.2649T>G