Canonical Allele Identifier: PA2826463181
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231618
ClinVar RCV Id: RCV000219363 RCV002515630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Thr168Arg
CA10577945
NM_001258281.1:c.503C>G