Canonical Allele Identifier: PA2741884589
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2941305
ClinVar RCV Id: RCV003792567

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.His924Pro
CA369193214
NM_001458.5:c.2771A>C