Canonical Allele Identifier: PA658812788
Gene: FBN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 528417
ClinVar RCV Id: RCV000633606
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001990.2:p.Cys1352Trp
CA360756957
NM_001999.4:c.4056T>G