ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA207693
Gene: LMNA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
66828
ClinVar RCV Id:
RCV000057301
ClinVar Variation Id:
66829
ClinVar RCV Id:
RCV000057302
RCV000193901
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_733822.1:p.Lys486Asn
CA017278
NM_170708.4:c.1458G>C
CA017283
NM_170708.4:c.1458G>T