Canonical Allele Identifier: PA2741884782
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 2937220
ClinVar RCV Id: RCV003791410

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Thr2564Ser
CA369219688
NM_001458.5:c.7690A>T
CA369219695
NM_001458.5:c.7691C>G