Canonical Allele Identifier: PA2826658069
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66828
ClinVar RCV Id: RCV000057301
ClinVar Variation Id: 66829
ClinVar RCV Id: RCV000057302 RCV000193901
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Lys405Asn
CA017278
NM_001282624.2:c.1215G>C
CA017283
NM_001282624.2:c.1215G>T