Canonical Allele Identifier: PA2826657884
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_001269553.1:p.Ser314Trp
CA342820931
NM_001282624.2:c.941C>G