Allele Registry

Canonical Allele Identifier: PA094766

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV000007614

RCV000506655

RCV001009472

RCV001269654

RCV003473038

ClinVar Variation:

7193

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Thr338Ile	CA325581 NM_000492.4:c.1013C>T