Canonical Allele Identifier: PA281832
Gene: FBN1 HGNC NCBI
ClinVar RCV:
RCV000029763
ClinVar Variation:
36101
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000129.3:p.Trp217Gly
CA016532
NM_000138.5:c.649T>G