Canonical Allele Identifier: PA294501
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90569
ClinVar RCV Id: RCV000132166 RCV000212599 RCV000411777 RCV000781558 RCV000765665 RCV001083003 RCV001356152 RCV001798264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg406Gln
CA017527
NM_000251.3:c.1217G>A