Canonical Allele Identifier: PA891850124
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 577268
ClinVar RCV Id: RCV000699970 RCV001585646 RCV002388303 RCV002485715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Arg2553Trp
CA4476333
NM_001458.5:c.7657C>T