Canonical Allele Identifier: PA357476
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 220024
ClinVar RCV Id: RCV000204877 RCV000491044 RCV001570632 RCV003997603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala848Ser
CA036472
NM_000251.3:c.2542G>T