Canonical Allele Identifier: PA915982713
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48070
ClinVar RCV Id: RCV000055999 RCV000057427 RCV000211790 RCV000618699 RCV000653912 RCV001824588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Glu91Lys
CA018291
NM_001257374.3:c.271G>A