Canonical Allele Identifier: PA322169
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 213511
ClinVar RCV Id: RCV000197706 RCV002229481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Arg2643Cys
CA322167
NM_001110556.2:c.7927C>T