Canonical Allele Identifier: PA2826659138
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1052547
ClinVar RCV Id: RCV001360754

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Pro391Ala
CA342820834
NM_001282625.2:c.1171C>G