Allele Registry

Canonical Allele Identifier: PA094890

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV000577097

RCV001509322

ClinVar Variation:

53558

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Tyr917Cys	CA326911 NM_000492.4:c.2750A>G