Allele Registry

Canonical Allele Identifier: PA2826443635

Gene: LMNA HGNC NCBI

Linked Data

ClinVar RCV:

RCV000621062

RCV000808964

RCV001096939

RCV001096940

RCV001096941

RCV001096942

RCV001096943

RCV001096944

RCV001096945

RCV001096946

RCV001102354

RCV001102355

RCV001190252

RCV001544605

RCV004002668

ClinVar Variation:

519022

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Val330Met	CA049885 NM_001257374.3:c.988G>A