Canonical Allele Identifier: PA2580119069
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1791569
ClinVar RCV Id: RCV002430716
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ile820Val
CA368981438
NM_000492.4:c.2458A>G