Canonical Allele Identifier: PA2826659200
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66798
ClinVar RCV Id: RCV000057261 RCV000694118 RCV000772169 RCV002444514 RCV003996501 RCV002281901
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Leu421Pro
CA016923
NM_001282625.2:c.1262T>C