Canonical Allele Identifier: PA2826463630
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90503
ClinVar RCV Id: RCV000500876 RCV002345383 RCV002228181 RCV003452795
ClinVar Variation Id: 232810
ClinVar RCV Id: RCV000218258 RCV000255930 RCV001232403 RCV003454644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly272Arg
CA016843
NM_001258281.1:c.814G>A
CA10577964
NM_001258281.1:c.814G>C