Canonical Allele Identifier: PA1139673178
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 952392
ClinVar RCV Id: RCV001224498
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Ser2615Gly
CA337272560
NM_001110556.2:c.7843A>G