Canonical Allele Identifier: PA2826657870
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 408997
ClinVar RCV Id: RCV000476791 RCV001753890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg307_Pro312dup
CA16609880
NM_001282624.2:c.918_935dup