Canonical Allele Identifier: PA2826465611
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1791577
ClinVar RCV Id: RCV002430717 RCV003101842
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly754Arg
CA346730322
NM_001258281.1:c.2260G>C