Canonical Allele Identifier: PA658809028
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 539343
ClinVar RCV Id: RCV000649070
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Lys2576Thr
CA369219851
NM_001458.5:c.7727A>C