Canonical Allele Identifier: PA915982048
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 625948
ClinVar RCV Id: RCV000767979

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Phe1438Leu
CA415217388
NM_001456.4:c.4314C>G
CA415217391
NM_001456.4:c.4314C>A
CA415217420
NM_001456.4:c.4312T>C