Canonical Allele Identifier: PA2826658391
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1341358
ClinVar RCV Id: RCV001829276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Asn56Lys
CA342808066
NM_001282625.2:c.168C>A
CA342808067
NM_001282625.2:c.168C>G