Canonical Allele Identifier: PA2826660362
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14495
ClinVar RCV Id: RCV000503996 RCV000547164 RCV000681569 RCV000057235 RCV001089610 RCV002321484 RCV003319170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg377His
CA016651
NM_001282626.2:c.1130G>A