Canonical Allele Identifier: PA2573164927
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1426650
ClinVar RCV Id: RCV001949777 RCV002442883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln288His
CA346732864
NM_000251.3:c.864G>C
CA346732865
NM_000251.3:c.864G>T