Canonical Allele Identifier: PA2826660290
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66762
ClinVar RCV Id: RCV000057218 RCV000500548 RCV000653911 RCV000845011 RCV000754811 RCV002504959 RCV003996495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg349Trp
CA016479
NM_001282626.2:c.1045C>T