Canonical Allele Identifier: PA2825611871
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1914760
ClinVar RCV Id: RCV002612825

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Thr933Ser
CA369193301
NM_001127487.2:c.2797A>T
CA369193303
NM_001127487.2:c.2798C>G