Canonical Allele Identifier: PA101826
Gene: FBN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 520
ClinVar RCV Id: RCV000000549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001990.2:p.Glu391Lys
CA281513
NM_001999.4:c.1171G>A