Canonical Allele Identifier: PA891850125
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 549664
ClinVar RCV Id: RCV000714272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Tyr2563Cys
CA369219679
NM_001458.5:c.7688A>G