Canonical Allele Identifier: PA645429317
Gene: FSCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 377132
ClinVar RCV Id: RCV000423345 RCV000764149 RCV004022273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070650.1:p.Val277Ile
CA8836893
NM_001077182.3:c.829G>A