Canonical Allele Identifier: PA2826660406
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 3071835
ClinVar RCV Id: RCV004016329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Ser395Trp
CA342820931
NM_001282626.2:c.1184C>G