Canonical Allele Identifier: PA2826660112
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 518473
ClinVar RCV Id: RCV000622065 RCV001301578 RCV001181566 RCV003133403 RCV002476374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Leu263Met
CA342817408
NM_001282626.2:c.787C>A