Canonical Allele Identifier: PA2826660581
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14489
ClinVar RCV Id: RCV000015579 RCV000057298 RCV001174239 RCV001248961 RCV001235764 RCV002390112 RCV002482872 RCV004532362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg482Trp
CA017258
NM_001282626.2:c.1444C>T