Canonical Allele Identifier: PA2829332943
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 3221724
ClinVar RCV Id: RCV004511048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Ala1174Thr
CA369197150
NM_001458.5:c.3520G>A