ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826657614
Gene: LMNA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
435769
ClinVar RCV Id:
RCV000503745
RCV001382395
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001269553.1:p.Ala197Pro
CA342817513
NM_001282624.2:c.589G>C