Canonical Allele Identifier: PA2573217831
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1420243
ClinVar RCV Id: RCV001943495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Gly2072Arg
CA369211816
NM_001458.5:c.6214G>A
CA369211817
NM_001458.5:c.6214G>C