Canonical Allele Identifier: PA207416
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 211012

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Thr835Met
CA207414
NM_001456.4:c.2504C>T