Canonical Allele Identifier: PA2573217850
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1367236

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Arg2206Trp
CA166191170
NM_001458.5:c.6616C>T