Canonical Allele Identifier: PA2826658155
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 435773
ClinVar RCV Id: RCV000500844 RCV000697810
ClinVar Variation Id: 581796
ClinVar RCV Id: RCV000705726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Leu449Phe
CA342823527
NM_001282624.2:c.1345C>T
CA891842720
NM_001282624.2:c.1344_1345delinsCT