Canonical Allele Identifier: PA2825614495
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2112094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Ile2127Thr
CA369212634
NM_001127487.2:c.6380T>C