Allele Registry

Canonical Allele Identifier: PA2826442759

Gene: LMNA HGNC NCBI

ClinVar Allele:

57231

ClinVar RCV:

RCV000041350

RCV000057407

RCV001265661

RCV001852841

ClinVar Variation:

48067

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Thr38Pro	CA018114 NM_001257374.3:c.112A>C