Allele Registry

Canonical Allele Identifier: PA2826443341

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000144027

RCV001243750

RCV002483277

RCV003998157

ClinVar Variation:

155896

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Met236Ile	CA016471 NM_001257374.3:c.708G>T CA342820261 NM_001257374.3:c.708G>A CA342820262 NM_001257374.3:c.708G>C