Allele Registry

Canonical Allele Identifier: PA326683

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV000577395

ClinVar Variation:

53392

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Ile601Thr	CA326682 NM_000492.4:c.1802T>C