Canonical Allele Identifier: PA2826658370
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 246300
ClinVar RCV Id: RCV000235498
ClinVar Variation Id: 1709835
ClinVar RCV Id: RCV002290177
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Val49Leu
CA10584110
NM_001282625.2:c.145G>C
CA342807952
NM_001282625.2:c.145G>T