Allele Registry

Canonical Allele Identifier: PA325692

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV000029477

RCV000727666

RCV001004225

RCV002284179

RCV003473126

ClinVar Variation:

35824

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Pro5Leu	CA325691 NM_000492.4:c.14C>T