Canonical Allele Identifier: PA2826657598
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_001269553.1:p.Tyr186His
CA018657
NM_001282624.2:c.556T>C