Canonical Allele Identifier: PA2826657488
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 264626
ClinVar RCV Id: RCV000247356 RCV000594818 RCV000800454 RCV001179387 RCV003995736
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg139Cys
CA054046
NM_001282624.2:c.415C>T