Canonical Allele Identifier: PA2826658503
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 520647
ClinVar RCV Id: RCV000622678 RCV001376156 RCV003133407
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Leu102Pro
CA342808708
NM_001282625.2:c.305T>C