Canonical Allele Identifier: PA2826464966
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182597
ClinVar RCV Id: RCV000160637 RCV001013808 RCV003998486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu592Gly
CA019625
NM_001258281.1:c.1775A>G