Canonical Allele Identifier: PA2830325727
Gene: LMNA HGNC NCBI
ClinVar RCV:
RCV001313361
ClinVar Variation:
1014606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Arg11Leu
CA342806869
NM_170707.4:c.32G>T