Canonical Allele Identifier: PA2826657552
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14524
ClinVar RCV Id: RCV000201142 RCV000814531 RCV000015621 RCV000057452
ClinVar Variation Id: 543181
ClinVar RCV Id: RCV000653857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg168Trp
CA018559
NM_001282624.2:c.502C>T
CA658795529
NM_001282624.2:c.501_502delinsTT