Canonical Allele Identifier: PA1139700956
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 948527
ClinVar RCV Id: RCV001219798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Ala797Ser
CA415237182
NM_001456.4:c.2389G>T