Canonical Allele Identifier: PA2826443998
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48049
ClinVar RCV Id: RCV000041330 RCV000057355 RCV001065506 RCV001184222 RCV002467559 RCV002504919 RCV003162351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Arg472His
CA020327
NM_001257374.3:c.1415G>A