Canonical Allele Identifier: PA2826657499
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 41234
ClinVar RCV Id: RCV000034134 RCV000190400 RCV001178806 RCV001781340 RCV001384595 RCV003996150 RCV001814022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg144Gln
CA018437
NM_001282624.2:c.431G>A