Canonical Allele Identifier: PA2826465728
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408542
ClinVar RCV Id: RCV002230812 RCV003470450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu787del
CA1649293
NM_001258281.1:c.2359_2361del