Canonical Allele Identifier: PA2826660135
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 435769
ClinVar RCV Id: RCV000503745 RCV001382395
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Ala278Pro
CA342817513
NM_001282626.2:c.832G>C