Canonical Allele Identifier: PA891846890
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 570930
ClinVar RCV Id: RCV000691925 RCV004025104
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val57Gly
CA346728990
NM_000251.3:c.170T>G