Allele Registry

Canonical Allele Identifier: PA2830327291

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV003581262

ClinVar Variation:

2728396

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Met352Thr	CA342820281 NM_170707.4:c.1055T>C