Canonical Allele Identifier: PA915982636
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66907
ClinVar RCV Id: RCV000057418
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Arg77Pro
CA018239
NM_001257374.3:c.230_231delinsCC
CA342816883
NM_001257374.3:c.230G>C