Canonical Allele Identifier: PA2826659779
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 522979
ClinVar RCV Id: RCV000626177 RCV001186690 RCV003106008 RCV004002756
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg110His
CA052231
NM_001282626.2:c.329G>A