Canonical Allele Identifier: PA2826658352
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 374201
ClinVar RCV Id: RCV000415420 RCV001861451
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Val44Phe
CA16043361
NM_001282625.2:c.130G>T