Canonical Allele Identifier: PA2579922068
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773618
ClinVar RCV Id: RCV003584474 RCV003759892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile794Val
CA346730097
NM_000251.3:c.2380A>G