Canonical Allele Identifier: PA2580262568
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1914760
ClinVar RCV Id: RCV002612825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Thr933Ser
CA369193301
NM_001458.5:c.2797A>T
CA369193303
NM_001458.5:c.2798C>G