Canonical Allele Identifier: PA658678573
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 472079
ClinVar RCV Id: RCV000550050 RCV002497176 RCV004024194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Thr1597Met
CA4475458
NM_001458.5:c.4790C>T