Canonical Allele Identifier: PA217775
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66778
ClinVar RCV Id: RCV000057236 RCV001237945 RCV002321554 RCV003448256 RCV003996497
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Arg377Leu
CA016657
NM_170708.4:c.1130G>T