Canonical Allele Identifier: PA094184
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 7142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly551Ser
CA325536
NM_000492.4:c.1651G>A