Canonical Allele Identifier: PA2826660671
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14513
ClinVar RCV Id: RCV000057332 RCV000015608 RCV002399329 RCV002467496 RCV003234906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Ala529Val
CA017534
NM_001282626.2:c.1586C>T