ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826659330
Gene: LMNA
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000057301
RCV000057302
RCV000193901
ClinVar Variation:
66828
66829
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001269554.1:p.Lys486Asn
CA017278
NM_001282625.2:c.1458G>C
CA017283
NM_001282625.2:c.1458G>T