Canonical Allele Identifier: PA915981028
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 11766
ClinVar RCV Id: RCV000012532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.Asp203Tyr
CA256060
NM_001456.4:c.607G>T