Allele Registry

Canonical Allele Identifier: PA1139700679

Gene: FLNA HGNC NCBI

ClinVar RCV:

RCV001209765

ClinVar Variation:

940228

HGVS (amino-acid)	Matching Registered Transcripts
NP_001447.2:p.Pro207Gln	CA415248967 NM_001456.4:c.620C>A