Canonical Allele Identifier: PA658808732
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 539420
ClinVar RCV Id: RCV000649154 RCV000786311 RCV002406443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val601Ala
CA4474480
NM_001458.5:c.1802T>C