Canonical Allele Identifier: PA645405738
Gene: FBN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 406360
ClinVar RCV Id: RCV000476981

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000129.3:p.Asn1907Ser
CA16614507
NM_000138.5:c.5720A>G