Canonical Allele Identifier: PA2825557503
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 426758
ClinVar RCV Id: RCV000489668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Gly132Arg
CA415251014
NM_001110556.2:c.394G>C
CA415251018
NM_001110556.2:c.394G>A