Canonical Allele Identifier: PA645381757
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 393067
ClinVar RCV Id: RCV000423665
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Pro17Leu
CA16608787
NM_001456.4:c.50C>T