Canonical Allele Identifier: PA103632
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14487
ClinVar RCV Id: RCV000015576 RCV000057324 RCV000192011 RCV001185736 RCV001223656 RCV002288492 RCV003319169 RCV003996098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Arg527Cys
CA017487
NM_170707.4:c.1579C>T