Canonical Allele Identifier: PA658682622
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 464978
ClinVar RCV Id: RCV000535719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Asn829Asp
CA415236379
NM_001456.4:c.2485A>G