Canonical Allele Identifier: PA658759386
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 488377
ClinVar RCV Id: RCV000578163

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Asn770Ser
CA415237538
NM_001456.4:c.2309A>G