Canonical Allele Identifier: PA100521
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 11773
ClinVar RCV Id: RCV000012540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Cys210Phe
CA256064
NM_001110556.2:c.629G>T