Canonical Allele Identifier: PA176594
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 163866
ClinVar RCV Id: RCV000150939 RCV000653861 RCV000732765 RCV000771896 RCV002336298 RCV002505147 RCV003998206
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Arg166Gln
CA018161
NM_170707.4:c.497G>A