Canonical Allele Identifier: PA2573217825
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1447193
ClinVar RCV Id: RCV001996734
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Ile2038Met
CA369211272
NM_001458.5:c.6114C>G