Canonical Allele Identifier: PA2826660382
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 245758
ClinVar RCV Id: RCV000236639 RCV002518430
ClinVar Variation Id: 934438
ClinVar RCV Id: RCV001202827
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg386Ser
CA10584129
NM_001282626.2:c.1158G>C
CA342820750
NM_001282626.2:c.1158G>T