Canonical Allele Identifier: PA324964
Gene: FLNA HGNC NCBI

Linked Data

ClinVar Variation Id: 213448
ClinVar RCV Id: RCV001705110 RCV001057778
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001447.2:p.His1443Asn
CA324962
NM_001456.4:c.4327C>A