Canonical Allele Identifier: PA209146
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 211017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Thr1506Ile
CA209144
NM_001456.4:c.4517C>T