Canonical Allele Identifier: PA2826463193
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455609
ClinVar RCV Id: RCV000535190 RCV002367769
ClinVar Variation Id: 2773602
ClinVar RCV Id: RCV003584458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asp170Glu
CA346732040
NM_001258281.1:c.510C>A
CA346732045
NM_001258281.1:c.510C>G