Canonical Allele Identifier: PA2826464976
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 525622
ClinVar RCV Id: RCV000629738 RCV001179138 RCV004002773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys595Glu
CA346728873
NM_001258281.1:c.1783A>G