Canonical Allele Identifier: PA2826660691
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1677884
ClinVar RCV Id: RCV002223565 RCV003089177
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Val538Ala
CA050838
NM_001282626.2:c.1613T>C