Canonical Allele Identifier: PA2826659100
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 429219
ClinVar RCV Id: RCV000493512
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Tyr376His
CA342820546
NM_001282625.2:c.1126T>C