Canonical Allele Identifier: PA2826659121
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 245758
ClinVar Variation Id: 934438
ClinVar RCV Id: RCV001202827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg386Ser
CA10584129
NM_001282625.2:c.1158G>C
CA342820750
NM_001282625.2:c.1158G>T