Canonical Allele Identifier: PA2825614634
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1367236

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Arg2173Trp
CA166191170
NM_001127487.2:c.6517C>T