Canonical Allele Identifier: PA658670729
Gene: FBN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 458775
ClinVar RCV Id: RCV000525229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001990.2:p.Glu2019Lys
CA360766610
NM_001999.4:c.6055G>A