Canonical Allele Identifier: PA658673247
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483684
ClinVar RCV Id: RCV000562070 RCV000629872 RCV004527663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Arg929Leu
CA346732210
NM_000251.3:c.2786G>T