Allele Registry

Canonical Allele Identifier: PA124057

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015600

RCV000057349

ClinVar Variation:

14506

HGVS (amino-acid)	Matching Registered Transcripts
NP_005563.1:p.Ala57Pro	CA017669 NM_005572.4:c.169G>C