Canonical Allele Identifier: PA2826657891
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 449052
ClinVar RCV Id: RCV000523012 RCV000695647 RCV002341216 RCV003532151 RCV004003591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg316His
CA049391
NM_001282624.2:c.947G>A