Allele Registry

Canonical Allele Identifier: PA327539

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV000577392

ClinVar Variation:

53978

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Lys166Glu	CA327538 NM_000492.4:c.496A>G