Canonical Allele Identifier: PA2580119097
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2182436
ClinVar RCV Id: RCV002610848

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asp828Gly
CA164948434
NM_000492.4:c.2483A>G