Canonical Allele Identifier: PA332431
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135859
ClinVar RCV Id: RCV000122987 RCV000411448 RCV000563636 RCV003149838 RCV002469017 RCV003997407
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys872Arg
CA020814
NM_000251.3:c.2615A>G