Allele Registry

Canonical Allele Identifier: PA294577

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000144027

RCV001243750

RCV002483277

RCV003998157

ClinVar Variation:

155896

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Met348Ile	CA016471 NM_170707.4:c.1044G>T CA342820261 NM_170707.4:c.1044G>A CA342820262 NM_170707.4:c.1044G>C