Canonical Allele Identifier: PA321589
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 213485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Pro2423Ser
CA321587
NM_001110556.2:c.7267C>T