Canonical Allele Identifier: PA658660598
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 457185
ClinVar RCV Id: RCV000524595
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000129.3:p.Gly985Trp
CA392329497
NM_000138.5:c.2953G>T