Canonical Allele Identifier: PA2826465237
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 232677
ClinVar RCV Id: RCV000214268 RCV000524727 RCV004532799
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys654Glu
CA034415
NM_001258281.1:c.1960A>G