Canonical Allele Identifier: PA2826657665
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_001269553.1:p.Arg217Leu
CA342817797
NM_001282624.2:c.650G>T