Canonical Allele Identifier: PA915982642
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66910
ClinVar RCV Id: RCV000057421 RCV000653887 RCV000619042 RCV000768712 RCV001449792 RCV003447483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Arg78Gln
CA018251
NM_001257374.3:c.233G>A