Canonical Allele Identifier: PA2826657940
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66798
ClinVar RCV Id: RCV000057261 RCV000694118 RCV000772169 RCV002444514 RCV003996501 RCV002281901
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Leu340Pro
CA016923
NM_001282624.2:c.1019T>C