Canonical Allele Identifier: PA2826465955
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 187449
ClinVar RCV Id: RCV000167178 RCV000706985 RCV001356340 RCV003995570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Ile840Arg
CA020901
NM_001258281.1:c.2519T>G