Canonical Allele Identifier: PA100696
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 193845
ClinVar RCV Id: RCV000174052 RCV000490438 RCV000755539 RCV001079269 RCV004020064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Val528Met
CA302718
NM_001110556.2:c.1582G>A