Canonical Allele Identifier: PA2826660667
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66850
ClinVar RCV Id: RCV000057329 RCV000472329 RCV000499741 RCV001814041 RCV003483458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Thr528Arg
CA017510
NM_001282626.2:c.1583C>G