Canonical Allele Identifier: PA123998
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14486
ClinVar RCV Id: RCV000015575 RCV000041318 RCV000057299 RCV000190399 RCV000459624 RCV000754814 RCV000763258 RCV001179839 RCV001822996 RCV002390111 RCV004532361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Arg482Gln
CA014814
NM_005572.4:c.1445G>A