Canonical Allele Identifier: PA2826463323
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182600
ClinVar RCV Id: RCV000160640 RCV000798669 RCV001184011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln198Arg
CA022268
NM_001258281.1:c.593A>G