Canonical Allele Identifier: PA2826660348
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 498978
ClinVar RCV Id: RCV000592581 RCV000696116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Glu372Lys
CA342820494
NM_001282626.2:c.1114G>A