Canonical Allele Identifier: PA274735
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 190193
ClinVar RCV Id: RCV000170413 RCV000640771 RCV001442515 RCV002321679
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Asp1354Asn
CA274734
NM_001110556.2:c.4060G>A