Canonical Allele Identifier: PA2579922519
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_000242.1:p.Gly820Arg
CA346730322
NM_000251.3:c.2458G>C