Canonical Allele Identifier: PA346438
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 180404
ClinVar RCV Id: RCV000157292 RCV002362839
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Phe237Ser
CA018485
NM_170708.4:c.710T>C