Canonical Allele Identifier: PA094658
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 7217

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ser1251Asn
CA325603
NM_000492.4:c.3752G>A