Canonical Allele Identifier: PA645464820
Gene: FBN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 411815
ClinVar RCV Id: RCV000473636

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001990.2:p.Gly1172Asp
CA16611897
NM_001999.4:c.3515G>A