Canonical Allele Identifier: PA658672880
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486870
ClinVar RCV Id: RCV000566809 RCV000781556 RCV001069626 RCV001355386
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly669Cys
CA346728968
NM_000251.3:c.2005G>T