Canonical Allele Identifier: PA164877
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141236
ClinVar RCV Id: RCV000129653 RCV001047553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.His783Arg
CA020486
NM_000251.3:c.2348A>G