Canonical Allele Identifier: PA2825615209
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1482518
ClinVar RCV Id: RCV001995665

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Ala2557Ser
CA369219959
NM_001127487.2:c.7669G>T