Allele Registry

Canonical Allele Identifier: PA2826657468

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV002043590

ClinVar Variation:

1518907

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Ile129Thr	CA342817078 NM_001282624.2:c.386T>C