Canonical Allele Identifier: PA093631
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 35866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Arg1070Gln
CA275095
NM_000492.4:c.3209G>A