ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826443850
Gene: LMNA
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000041324
RCV000057323
RCV000182372
RCV000245950
RCV000474372
RCV000678714
RCV001181346
RCV001250579
RCV001330499
RCV003996456
RCV003996716
ClinVar Variation:
48045
200946
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001244303.1:p.Gly411Arg
CA017464
NM_001257374.3:c.1231G>A
CA017471
NM_001257374.3:c.1231G>C