Canonical Allele Identifier: PA322092
Gene: FBN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 213260

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001990.2:p.Thr26Ala
CA322091
NM_001999.4:c.76A>G