Canonical Allele Identifier: PA1139703605
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 864174
ClinVar RCV Id: RCV001071297

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Thr1514Met
CA369201977
NM_001458.5:c.4541C>T