ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826442714
Gene: LMNA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
14488
ClinVar RCV Id:
RCV000015577
RCV000015578
RCV000057399
RCV001387326
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001244303.1:p.Arg21Leu
CA018044
NM_001257374.3:c.62G>T