Canonical Allele Identifier: PA210134
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 208878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Glu2635Lys
CA210133
NM_001110556.2:c.7903G>A