Canonical Allele Identifier: PA2826657535
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 634638
ClinVar RCV Id: RCV000785172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Asp162Tyr
CA342817279
NM_001282624.2:c.484G>T