Canonical Allele Identifier: PA217837
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66792
ClinVar RCV Id: RCV000057253 RCV000157294 RCV001056678 RCV002336206 RCV002483088 RCV003996499
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Ser395Leu
CA016823
NM_170708.4:c.1184C>T