Canonical Allele Identifier: PA2826464854
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 455532
ClinVar RCV Id: RCV000547904 RCV000568306 RCV001572130 RCV002481753 RCV004003740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Arg565Lys
CA346728562
NM_001258281.1:c.1694G>A