Canonical Allele Identifier: PA321037
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 213513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Thr167Asn
CA321035
NM_001456.4:c.500C>A