Canonical Allele Identifier: PA093831
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 196277

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Arg74Trp
CA275167
NM_000492.4:c.220C>T