Canonical Allele Identifier: PA2826658259
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2140137
ClinVar RCV Id: RCV003052963 RCV003134603 RCV003533333 RCV004009309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Ala9Thr
CA342806038
NM_001282625.2:c.25G>A