Canonical Allele Identifier: PA1139673040
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 963022
ClinVar RCV Id: RCV001236986

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Gly2027Ser
CA415196296
NM_001110556.2:c.6079G>A