Canonical Allele Identifier: PA658803818
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 502799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Glu588Gly
CA4451078
NM_000492.4:c.1763A>G