Canonical Allele Identifier: PA2826658682
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_001269554.1:p.Arg190Gln
CA018251
NM_001282625.2:c.569G>A