Canonical Allele Identifier: PA645472215
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408531
ClinVar RCV Id: RCV001358282 RCV001027097 RCV002230810 RCV003470449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ser268Leu
CA040677
NM_000251.3:c.803C>T