Canonical Allele Identifier: PA2826657743
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 246074
ClinVar RCV Id: RCV000653901 RCV000771975 RCV000727308 RCV001174248 RCV002401922 RCV003998912
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg254Gln
CA048759
NM_001282624.2:c.761G>A