Canonical Allele Identifier: PA2826657769
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2860240
ClinVar RCV Id: RCV003743173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg268Gln
CA342820264
NM_001282624.2:c.803G>A