Canonical Allele Identifier: PA2826658766
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 180115
ClinVar RCV Id: RCV000156919 RCV000538272 RCV001525549 RCV003152686 RCV003998328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Ile229Thr
CA018453
NM_001282625.2:c.686T>C