Allele Registry

Canonical Allele Identifier: PA915957384

Gene: CFTR HGNC NCBI

ClinVar Variation Id: 801154

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Phe1107Leu	CA368992523 NM_000492.4:c.3319T>C CA368992532 NM_000492.4:c.3321T>A CA368992534 NM_000492.4:c.3321T>G