Canonical Allele Identifier: PA915981066
Gene: FLNA HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Cys210Phe
CA256064
NM_001456.4:c.629G>T