Canonical Allele Identifier: PA103883
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14504
ClinVar RCV Id: RCV000015598 RCV000057409 RCV000211788 RCV000687241 RCV003318333 RCV004018635 RCV001170451
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Glu161Lys
CA018140
NM_170707.4:c.481G>A