Canonical Allele Identifier: PA2826659602
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 447702
ClinVar RCV Id: RCV000518408 RCV000653844
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg41Leu
CA342807753
NM_001282626.2:c.122G>T