Canonical Allele Identifier: PA1139701047
Gene: FBN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 840657
ClinVar RCV Id: RCV001042699
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001990.2:p.Asp1410Asn
CA360754215
NM_001999.4:c.4228G>A