Canonical Allele Identifier: PA2829603568
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2504491
ClinVar RCV Id: RCV003231952
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Asp357Gly
CA342820315
NM_005572.4:c.1070A>G