Canonical Allele Identifier: PA218252
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14508
ClinVar RCV Id: RCV000015602 RCV000057398 RCV000686691
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Arg133Pro
CA018038
NM_170708.4:c.398G>C