Canonical Allele Identifier: PA321869
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 213503

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Lys975Asn
CA321868
NM_001110556.2:c.2925G>C
CA415231386
NM_001110556.2:c.2925G>T