Canonical Allele Identifier: PA2826660668
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66849
ClinVar RCV Id: RCV000057328 RCV000201062 RCV001045262 RCV000986432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Thr528Lys
CA017504
NM_001282626.2:c.1583C>A