Allele Registry

Canonical Allele Identifier: PA2826657778

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV003581262

ClinVar Variation:

2728396

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Met271Thr	CA342820281 NM_001282624.2:c.812T>C