Canonical Allele Identifier: PA2826465969
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 216358
ClinVar RCV Id: RCV000197107 RCV000491688 RCV001550881 RCV001798670 RCV003997022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys843Arg
CA037327
NM_001258281.1:c.2528A>G