Canonical Allele Identifier: PA2826657507
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14518
ClinVar RCV Id: RCV000015615 RCV000057443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Asp149Asn
CA018460
NM_001282624.2:c.445G>A