Canonical Allele Identifier: PA1139705102
Gene: FLNC HGNC NCBI

Linked Data

ClinVar Variation Id: 937187
ClinVar RCV Id: RCV001206150
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001449.3:p.Pro2556Ser
CA4476335
NM_001458.5:c.7666C>T