Canonical Allele Identifier: PA2825615201
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760424

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Ile2550Thr
CA369219911
NM_001127487.2:c.7649T>C