Canonical Allele Identifier: PA658676299
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 465022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Pro2519Ser
CA10559870
NM_001110556.2:c.7555C>T