Canonical Allele Identifier: PA100608
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 11752
ClinVar RCV Id: RCV000012518 RCV001753412 RCV001857335 RCV002273924
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Leu656Phe
CA256053
NM_001110556.2:c.1966C>T