Canonical Allele Identifier: PA190593
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 184961
ClinVar RCV Id: RCV000164307 RCV001059239 RCV001762366 RCV003467289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala649Thr
CA019600
NM_000251.3:c.1945G>A