Canonical Allele Identifier: PA2826660564
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 36476
ClinVar RCV Id: RCV000030148 RCV000057294 RCV000154177 RCV000621248 RCV000653872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg471His
CA017220
NM_001282626.2:c.1412G>A