Canonical Allele Identifier: PA2499232906
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1009171

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Thr351Ala
CA368978902
NM_000492.4:c.1051A>G