Canonical Allele Identifier: PA915966605
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 650519
ClinVar RCV Id: RCV000805682 RCV001024434 RCV002291700
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Phe19Ser
CA346728591
NM_000251.3:c.56T>C