ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA217859
Gene: LMNA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
66797
ClinVar RCV Id:
RCV000057260
RCV000534245
RCV000764982
RCV001191555
RCV002381362
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_733821.1:p.Val415Ile
CA016913
NM_170707.4:c.1243G>A