Canonical Allele Identifier: PA2826465702
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90995
ClinVar RCV Id: RCV000215108 RCV000524393 RCV000662762 RCV001030485 RCV001174808 RCV003997164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys779Glu
CA020689
NM_001258281.1:c.2335A>G