Canonical Allele Identifier: PA094613
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91243
ClinVar RCV Id: RCV000076748 RCV000115547 RCV000148633 RCV000656876 RCV001084038 RCV001193245 RCV004542749 RCV003492427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala305Thr
CA022539
NM_000251.3:c.913G>A