Canonical Allele Identifier: PA2826465672
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_001245210.1:p.His773Arg
CA020662
NM_001258281.1:c.2318A>G