Canonical Allele Identifier: PA2825615169
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 577268

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Arg2520Trp
CA4476333
NM_001127487.2:c.7558C>T