Canonical Allele Identifier: PA321478
Gene: FBN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 213330
ClinVar RCV Id: RCV000197040 RCV001220936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001990.2:p.Asp1532Asn
CA321477
NM_001999.4:c.4594G>A