Canonical Allele Identifier: PA658812922
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 520647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Leu102Pro
CA342808708
NM_170708.4:c.305T>C