Canonical Allele Identifier: PA2826660648
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_001269555.1:p.Trp520Arg
CA342823343
NM_001282626.2:c.1558T>C
CA342823345
NM_001282626.2:c.1558T>A