Canonical Allele Identifier: PA2826660187
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 579396
ClinVar RCV Id: RCV000702673 RCV002485734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg298Leu
CA342817797
NM_001282626.2:c.893G>T