Canonical Allele Identifier: PA2580262674
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1707780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Pro1507Thr
CA369201930
NM_001458.5:c.4519C>A