Canonical Allele Identifier: PA2826463161
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1692296
ClinVar RCV Id: RCV002258507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys163Ile
CA346731884
NM_001258281.1:c.488A>T