Canonical Allele Identifier: PA262002
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48084
ClinVar RCV Id: RCV000041369 RCV000057461 RCV000617680 RCV002513583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Tyr267His
CA018657
NM_170708.4:c.799T>C