Canonical Allele Identifier: PA2826465768
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1996366
ClinVar RCV Id: RCV002802001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ser794Thr
CA346730981
NM_001258281.1:c.2380T>A