Canonical Allele Identifier: PA206362
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 211010
ClinVar RCV Id: RCV000193102 RCV001041470 RCV001566737 RCV002314817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Thr413Met
CA206360
NM_001456.4:c.1238C>T