Canonical Allele Identifier: PA284699
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66864
ClinVar RCV Id: RCV000057354 RCV000618100 RCV000653858 RCV001182287 RCV002504960 RCV003333022 RCV003996507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Ser553Leu
CA020320
NM_170708.4:c.1658C>T