Canonical Allele Identifier: PA645475194
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246114
ClinVar RCV Id: RCV000235402 RCV000561699 RCV000708838 RCV001854866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Pro670His
CA10584219
NM_000251.3:c.2009C>A