Canonical Allele Identifier: PA2499299751
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1014606
ClinVar RCV Id: RCV001313361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Arg11Leu
CA342806869
NM_170708.4:c.32G>T