Canonical Allele Identifier: PA2580262458
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1723749
ClinVar RCV Id: RCV002306310

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val234Gly
CA369221837
NM_001458.5:c.701T>G