Canonical Allele Identifier: PA2826465719
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1792886
ClinVar RCV Id: RCV002455810
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu783Gln
CA346730852
NM_001258281.1:c.2348T>A