Canonical Allele Identifier: PA2826464124
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455484
ClinVar RCV Id: RCV000567928 RCV000556329 RCV002476086 RCV003478112 RCV004003731
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Glu386Lys
CA46660139
NM_001258281.1:c.1156G>A