Canonical Allele Identifier: PA094936
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90990
ClinVar RCV Id: RCV000076492 RCV000166332 RCV000486446 RCV000765673 RCV000986690 RCV001085048 RCV001354097 RCV003153356 RCV004525868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.His839Arg
CA020662
NM_000251.3:c.2516A>G