Canonical Allele Identifier: PA2825612375
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 1948299
ClinVar RCV Id: RCV002685721
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120959.1:p.Thr1148Ser
CA369196908
NM_001127487.2:c.3442A>T
CA369196915
NM_001127487.2:c.3443C>G