Canonical Allele Identifier: PA282292
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 42436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000129.3:p.Cys2631Tyr
CA017451
NM_000138.5:c.7892G>A