Canonical Allele Identifier: PA2829604059
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 476824
ClinVar RCV Id: RCV000540642
ClinVar Variation Id: 943114
ClinVar RCV Id: RCV001213240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Trp520Arg
CA342823343
NM_005572.4:c.1558T>C
CA342823345
NM_005572.4:c.1558T>A