ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826660764
Gene: LMNA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
521983
ClinVar RCV Id:
RCV001524890
RCV002506519
RCV002533137
RCV002404709
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001269555.1:p.Arg582Leu
CA342826551
NM_001282626.2:c.1745G>T