Canonical Allele Identifier: PA2826657554
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66931
ClinVar RCV Id: RCV000057453 RCV000201012 RCV000501991 RCV000496185 RCV000548477 RCV000662104 RCV001814042 RCV003230389 RCV004018991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg168Gln
CA018567
NM_001282624.2:c.503G>A