Canonical Allele Identifier: PA915966613
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 665550
ClinVar RCV Id: RCV000823858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu51Val
CA346728954
NM_000251.3:c.151C>G