Canonical Allele Identifier: PA261949
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48029
ClinVar RCV Id: RCV000041306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Met371_Ala375del
CA016606
NM_170708.4:c.1111_1125del