Allele Registry

Canonical Allele Identifier: PA261982

Gene: LMNA HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

57240

ClinVar RCV:

RCV000041361

RCV000157293

RCV000182361

RCV000620828

RCV000770763

RCV000801882

RCV001174247

RCV001258043

RCV001798224

ClinVar Variation:

48076

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_005563.1:p.Ala242Val	CA018498 NM_005572.4:c.725C>T