Canonical Allele Identifier: PA658737709
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 491754
ClinVar RCV Id: RCV000583415 RCV001860086
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln397Arg
CA346733883
NM_000251.3:c.1190A>G