Canonical Allele Identifier: PA2826463209
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1507093
ClinVar RCV Id: RCV002011272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gln173Leu
CA346732096
NM_001258281.1:c.518A>T