Canonical Allele Identifier: PA100553
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 11756
ClinVar RCV Id: RCV000012522 RCV000178843 RCV001851804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Glu254Lys
CA221728
NM_001110556.2:c.760G>A