Canonical Allele Identifier: PA331721
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91270
ClinVar RCV Id: RCV000076775 RCV001554291 RCV003593904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu330Pro
CA022706
NM_000251.3:c.989T>C