Canonical Allele Identifier: PA2573217904
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1483054
ClinVar RCV Id: RCV002025333

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Val2592Phe
CA369219973
NM_001458.5:c.7774G>T