Canonical Allele Identifier: PA645471988
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 420794
ClinVar RCV Id: RCV000757471 RCV000775779 RCV001046068 RCV001824799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys248Arg
CA16617562
NM_000251.3:c.743A>G