Allele Registry

Canonical Allele Identifier: PA326542

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV000577045

RCV000731021

RCV003479674

ClinVar Variation:

53289

2682301

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Glu528Asp	CA326541 NM_000492.4:c.1584G>T CA368985063 NM_000492.4:c.1584G>C