Canonical Allele Identifier: PA645474394
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230562
ClinVar RCV Id: RCV000219613 RCV000483517 RCV000630079 RCV000986672 RCV002229222 RCV003997850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile497Val
CA028875
NM_000251.3:c.1489A>G