Canonical Allele Identifier: PA2826657741
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 36473
ClinVar RCV Id: RCV000030145 RCV000182368 RCV000546102 RCV000620788 RCV000721960 RCV000852407 RCV000845456 RCV000844672 RCV001196390 RCV003149579 RCV003492303 RCV002477025 RCV004532421
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg254Trp
CA016426
NM_001282624.2:c.760C>T