ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA124038
Gene: LMNA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
14499
ClinVar RCV Id:
RCV000148607
RCV000057326
RCV000555364
RCV001178367
RCV001174240
RCV002399328
RCV003996101
RCV000015592
RCV000015591
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_733822.1:p.Arg527His
CA014822
NM_170708.4:c.1580G>A