Canonical Allele Identifier: PA2826658153
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14482
ClinVar RCV Id: RCV000015571 RCV000057333
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Leu449Pro
CA017541
NM_001282624.2:c.1346T>C