ClinGen Allele Registry
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Canonical Allele Identifier:
PA916013532
Gene: LMNA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
14488
ClinVar RCV Id:
RCV000015577
RCV000015578
RCV000057399
RCV001387326
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001269553.1:p.Arg52Leu
CA018044
NM_001282624.2:c.155G>T