Canonical Allele Identifier: PA2826659616
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66815
ClinVar RCV Id: RCV000057281 RCV001230439
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Ile46Val
CA017105
NM_001282626.2:c.136A>G