Canonical Allele Identifier: PA645464783
Gene: FBN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 234773

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001990.2:p.Ser1102Gly
CA3395273
NM_001999.4:c.3304A>G