Canonical Allele Identifier: PA2826658018
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 178062
ClinVar RCV Id: RCV000154750 RCV000726125 RCV000824275 RCV001179779 RCV002381491 RCV003998270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Asn378Ser
CA017121
NM_001282624.2:c.1133A>G