Canonical Allele Identifier: PA2579924387
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1796064
ClinVar RCV Id: RCV002441438
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys931Ile
CA346732242
NM_000251.3:c.2792A>T