Canonical Allele Identifier: PA2826465488
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 619523
ClinVar RCV Id: RCV000758593 RCV001269395 RCV002442567 RCV003453545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Leu721Arg
CA346730002
NM_001258281.1:c.2162T>G