Canonical Allele Identifier: PA2826659190
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66797
ClinVar RCV Id: RCV000057260 RCV000534245 RCV000764982 RCV001191555 RCV002381362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Val415Ile
CA016913
NM_001282625.2:c.1243G>A