Canonical Allele Identifier: PA332433
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135860
ClinVar RCV Id: RCV000122988 RCV000412095 RCV001558333 RCV002251992 RCV000573859 RCV003997408 RCV004542928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile906Thr
CA020898
NM_000251.3:c.2717T>C