Canonical Allele Identifier: PA645475851
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 246167
ClinVar RCV Id: RCV000236795 RCV001857813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln846_Lys847del
CA10584224
NM_000251.3:c.2536_2541del