Canonical Allele Identifier: PA2826658143
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14499
ClinVar RCV Id: RCV000148607 RCV000057326 RCV000555364 RCV001178367 RCV001174240 RCV002399328 RCV003996101 RCV000015592 RCV000015591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg446His
CA014822
NM_001282624.2:c.1337G>A