Canonical Allele Identifier: PA2826659622
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 285548
ClinVar RCV Id: RCV000320512 RCV003987491
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Asp47Asn
CA10605149
NM_001282626.2:c.139G>A