Canonical Allele Identifier: PA2826658141
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14481
ClinVar RCV Id: RCV000015569 RCV000015570 RCV000700159 RCV000057327 RCV001375641 RCV004018633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg446Pro
CA017498
NM_001282624.2:c.1337G>C