Canonical Allele Identifier: PA322168
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 213511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Arg2635Cys
CA322167
NM_001456.4:c.7903C>T