Canonical Allele Identifier: PA2826464896
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1440576
ClinVar RCV Id: RCV001978891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val576Leu
CA346728676
NM_001258281.1:c.1726G>C