Canonical Allele Identifier: PA658690436
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 495561
ClinVar RCV Id: RCV000588784
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000129.3:p.Asp613Tyr
CA392340139
NM_000138.5:c.1837G>T