Canonical Allele Identifier: PA2826463013
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1483850
ClinVar RCV Id: RCV002003266 RCV002344166
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu124Val
CA039293
NM_001258281.1:c.370C>G