Canonical Allele Identifier: PA2830327498
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 435771
ClinVar RCV Id: RCV000501231

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Arg388Pro
CA342820778
NM_170707.4:c.1163G>C