Canonical Allele Identifier: PA103692
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14494
ClinVar RCV Id: RCV000015585 RCV000057353 RCV001068657 RCV001804734 RCV002399327 RCV004532363 RCV003996099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Arg582His
CA020309
NM_170707.4:c.1745G>A