Canonical Allele Identifier: PA2826659582
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66765
ClinVar RCV Id: RCV000057221 RCV000499410 RCV001231384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Leu35Pro
CA016503
NM_001282626.2:c.104T>C