Allele Registry

Canonical Allele Identifier: PA2573187314

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV002043590

ClinVar Variation:

1518907

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Ile98Thr	CA342817078 NM_001257374.3:c.293T>C