Canonical Allele Identifier: PA2826658203
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 286258
ClinVar RCV Id: RCV000334194 RCV000541582 RCV000622473 RCV000825772 RCV001172624 RCV001183038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Asp472Asn
CA050891
NM_001282624.2:c.1414G>A