Canonical Allele Identifier: PA323969
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 213507

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Asn1556Asp
CA323968
NM_001110556.2:c.4666A>G