Canonical Allele Identifier: PA103482
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66782
ClinVar RCV Id: RCV000057243 RCV003581572
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Arg386Lys
CA016734
NM_170707.4:c.1157G>A