Canonical Allele Identifier: PA100660
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 11761
ClinVar RCV Id: RCV000012527 RCV000414151 RCV002051782 RCV002228026
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Ser1186Leu
CA256058
NM_001110556.2:c.3557C>T