Canonical Allele Identifier: PA2826465791
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1512753
ClinVar RCV Id: RCV002018236 RCV004011141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Asp798Gly
CA346731036
NM_001258281.1:c.2393A>G