Canonical Allele Identifier: PA217797
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66782
ClinVar RCV Id: RCV000057243 RCV003581572
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Arg386Lys
CA016734
NM_170708.4:c.1157G>A