Canonical Allele Identifier: PA2826657493
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14492
ClinVar RCV Id: RCV000015583 RCV000057440 RCV002286398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.His141Tyr
CA018412
NM_001282624.2:c.421C>T