Canonical Allele Identifier: PA915984252
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483694
ClinVar RCV Id: RCV000575907 RCV001858299 RCV003451249
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Val82Glu
CA346730475
NM_001258281.1:c.245T>A