Canonical Allele Identifier: PA2826660267
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66758
ClinVar RCV Id: RCV000057214 RCV000225878 RCV002426615 RCV002483086 RCV003996492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg336Gln
CA016433
NM_001282626.2:c.1007G>A