Canonical Allele Identifier: PA2826659572
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 476837
ClinVar RCV Id: RCV000529491 RCV000785916
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Lys32Glu
CA342807424
NM_001282626.2:c.94A>G