Canonical Allele Identifier: PA891849600
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 190185

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Ser617Leu
CA274726
NM_001456.4:c.1850C>T