Canonical Allele Identifier: PA645381831
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 426758
ClinVar RCV Id: RCV000489668

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Gly132Arg
CA415251014
NM_001456.4:c.394G>C
CA415251018
NM_001456.4:c.394G>A