Allele Registry

Canonical Allele Identifier: PA658827287

Gene: CFTR HGNC NCBI

ClinVar Variation Id: 558463

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Cys1355Phe	CA4451621 NM_000492.4:c.4064G>T