Canonical Allele Identifier: PA217865
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66798
ClinVar RCV Id: RCV000057261 RCV000694118 RCV000772169 RCV002444514 RCV003996501 RCV002281901
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Leu421Pro
CA016923
NM_170707.4:c.1262T>C