Canonical Allele Identifier: PA2826463075
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 127648
ClinVar RCV Id: RCV000115537 RCV000196378 RCV000215932 RCV000411245 RCV002505033 RCV003997281
ClinVar Variation Id: 1751677
ClinVar RCV Id: RCV002360225
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly138Arg
CA021573
NM_001258281.1:c.412G>A
CA346731092
NM_001258281.1:c.412G>C