Canonical Allele Identifier: PA2826659721
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 200929
ClinVar RCV Id: RCV000182351 RCV001852311
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Glu84Asp
CA017807
NM_001282626.2:c.252G>C
CA342808461
NM_001282626.2:c.252G>T