Canonical Allele Identifier: PA299359
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182579
ClinVar RCV Id: RCV000160611 RCV000212618 RCV000542071 RCV000656881 RCV001357332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln793Glu
CA020523
NM_000251.3:c.2377C>G