Canonical Allele Identifier: PA218136
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Gly578Ser
CA015235
NM_170708.4:c.1732G>A