Canonical Allele Identifier: PA1139704692
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 950691
ClinVar RCV Id: RCV001222453
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Thr2177Ala
CA369212757
NM_001458.5:c.6529A>G