Allele Registry

Canonical Allele Identifier: PA326695

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV000507939

RCV000778818

ClinVar Variation:

53399

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.His609Leu	CA326694 NM_000492.4:c.1826A>T