Canonical Allele Identifier: PA915957259
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 801153
ClinVar RCV Id: RCV000985687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Tyr1014del
CA915945435
NM_000492.4:c.3040_3042del