Canonical Allele Identifier: PA2499260000
Gene: FBN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1018262
ClinVar RCV Id: RCV001317536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001990.2:p.Pro1303Leu
CA3395103
NM_001999.4:c.3908C>T