Canonical Allele Identifier: PA174406
Gene: FBN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 161589
ClinVar RCV Id: RCV000149125
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001990.2:p.Glu2059Asp
CA174405
NM_001999.4:c.6177A>C
CA360764577
NM_001999.4:c.6177A>T