Canonical Allele Identifier: PA103935
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14525
ClinVar RCV Id: RCV000015623 RCV000015622 RCV000057227 RCV000470514 RCV000502108 RCV001420791
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Glu358Lys
CA016555
NM_170707.4:c.1072G>A