Canonical Allele Identifier: PA2580262669
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1720571
ClinVar RCV Id: RCV002298289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Glu1492Ala
CA369201832
NM_001458.5:c.4475A>C