Canonical Allele Identifier: PA2826657437
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1750607
ClinVar RCV Id: RCV002355911 RCV003098072
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Gln117Arg
CA342816992
NM_001282624.2:c.350A>G