Canonical Allele Identifier: PA2826659027
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 155896
ClinVar RCV Id: RCV000144027 RCV001243750 RCV003998157 RCV002483277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Met348Ile
CA016471
NM_001282625.2:c.1044G>T
CA342820261
NM_001282625.2:c.1044G>A
CA342820262
NM_001282625.2:c.1044G>C