Canonical Allele Identifier: PA913194048
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 632754

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Thr164Ala
CA4450745
NM_000492.4:c.490A>G