Canonical Allele Identifier: PA1139700558
Gene: FBN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 946201
ClinVar RCV Id: RCV001217015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001990.2:p.Glu855Asp
CA360767524
NM_001999.4:c.2565A>T
CA360767525
NM_001999.4:c.2565A>C