Canonical Allele Identifier: PA274727
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 190185
ClinVar RCV Id: RCV000170405 RCV001657940 RCV002228616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104026.1:p.Ser617Leu
CA274726
NM_001110556.2:c.1850C>T