Canonical Allele Identifier: PA262029
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48098
ClinVar RCV Id: RCV000182367 RCV000593819 RCV000769727 RCV001071970 RCV002381325 RCV003235003 RCV003335073 RCV001265547
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Arg331Gln
CA018936
NM_005572.4:c.992G>A