Canonical Allele Identifier: PA100639
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 11755
ClinVar RCV Id: RCV000012521 RCV000415125 RCV001000894 RCV002509151 RCV002354156 RCV003764562 RCV004545725
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Pro207Leu
CA256056
NM_001110556.2:c.620C>T