Canonical Allele Identifier: PA319893
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 213508
ClinVar RCV Id: RCV000195541 RCV001316709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Ile1666Thr
CA319891
NM_001110556.2:c.4997T>C