Canonical Allele Identifier: PA645464877
Gene: FBN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 263631
ClinVar RCV Id: RCV000244735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001990.2:p.Met1320Val
CA3395097
NM_001999.4:c.3958A>G