Allele Registry

Canonical Allele Identifier: PA2826660299

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV003581262

ClinVar Variation:

2728396

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Met352Thr	CA342820281 NM_001282626.2:c.1055T>C