Canonical Allele Identifier: PA353711
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 440459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Thr360Lys
CA353710
NM_000492.4:c.1079C>A