Canonical Allele Identifier: PA2573217903
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1482518
ClinVar RCV Id: RCV001995665

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Ala2590Ser
CA369219959
NM_001458.5:c.7768G>T