ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2829603693
Gene: LMNA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
2894607
ClinVar RCV Id:
RCV003743519
RCV004005840
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005563.1:p.Ser390Phe
CA342820822
NM_005572.4:c.1169C>T