ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826657477
Gene: LMNA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
65764
ClinVar RCV Id:
RCV000056000
RCV000057438
RCV001382394
RCV002362688
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001269553.1:p.Leu134Pro
CA018372
NM_001282624.2:c.401T>C