Canonical Allele Identifier: PA891846884
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 582790
ClinVar RCV Id: RCV000706952 RCV000776681 RCV003460988 RCV003999779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val3Met
CA346728404
NM_000251.3:c.7G>A