Canonical Allele Identifier: PA163721
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 140843
ClinVar RCV Id: RCV000129044 RCV000199801 RCV000656877 RCV000662760 RCV003997475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu488Val
CA018364
NM_000251.3:c.1462T>G