Canonical Allele Identifier: PA321023
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 213465

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.His787Gln
CA321022
NM_001110556.2:c.2361C>G
CA415237345
NM_001110556.2:c.2361C>A