Allele Registry

Canonical Allele Identifier: PA2829603547

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV003581262

ClinVar Variation:

2728396

HGVS (amino-acid)	Matching Registered Transcripts
NP_005563.1:p.Met352Thr	CA342820281 NM_005572.4:c.1055T>C