Canonical Allele Identifier: PA103498
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14519
ClinVar RCV Id: RCV001174241 RCV000653937 RCV001257937 RCV001188431 RCV002336085 RCV000015616 RCV000057255
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Arg399Cys
CA016847
NM_170707.4:c.1195C>T