Canonical Allele Identifier: PA319892
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 213508
ClinVar RCV Id: RCV000195541 RCV001316709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Ile1658Thr
CA319891
NM_001456.4:c.4973T>C