Canonical Allele Identifier: PA299343
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182572
ClinVar RCV Id: RCV000160603 RCV000492028 RCV000629694 RCV003462091 RCV003998478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr724Met
CA020167
NM_000251.3:c.2171C>T