ClinGen Allele Registry
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Canonical Allele Identifier:
PA322639
Gene: FLNA
HGNC
NCBI
Linked Data
ClinVar Variation Id:
213463
ClinVar RCV Id:
RCV000844958
RCV001818466
RCV002317718
RCV001711508
RCV001853153
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001104026.1:p.Arg708Gln
CA322638
NM_001110556.2:c.2123G>A