Canonical Allele Identifier: PA2826658580
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14488
ClinVar RCV Id: RCV000015577 RCV000015578 RCV000057399 RCV001387326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg133Leu
CA018044
NM_001282625.2:c.398G>T