Canonical Allele Identifier: PA2826882238
Gene: CWF19L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 488455
ClinVar RCV Id: RCV001093418 RCV000578265
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290335.1:p.Glu382del
CA5646826
NM_001303406.2:c.1144_1146del