Allele Registry

Canonical Allele Identifier: PA326499

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV000577263

ClinVar Variation:

53263

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Gln493Arg	CA326498 NM_000492.4:c.1478A>G