Canonical Allele Identifier: PA2826463255
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483711
ClinVar RCV Id: RCV000568266 RCV000808962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys183Arg
CA346732298
NM_001258281.1:c.548A>G