Canonical Allele Identifier: PA103901
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14484
ClinVar RCV Id: RCV000015573 RCV000057428 RCV000211791 RCV003581565
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Glu203Gly
CA018298
NM_170707.4:c.608A>G