Canonical Allele Identifier: PA915954087
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 653460
ClinVar RCV Id: RCV000809239 RCV002406815
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro618Ser
CA346728431
NM_000251.3:c.1852C>T