Canonical Allele Identifier: PA2826660013
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 950917
ClinVar RCV Id: RCV001222732 RCV002366000 RCV003132287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg221His
CA054078
NM_001282626.2:c.662G>A