Canonical Allele Identifier: PA2826659982
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66916
ClinVar RCV Id: RCV000057431 RCV000694277 RCV002354249
ClinVar Variation Id: 636395
ClinVar RCV Id: RCV000788205 RCV002535769
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Phe206Leu
CA018318
NM_001282626.2:c.618C>G
CA342817045
NM_001282626.2:c.616T>C
CA342817050
NM_001282626.2:c.618C>A