Canonical Allele Identifier: PA891846913
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 577354
ClinVar RCV Id: RCV000700085 RCV001026881 RCV001811450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu262Val
CA346732502
NM_000251.3:c.785A>T