Allele Registry

Canonical Allele Identifier: PA326984

Gene: CFTR HGNC NCBI

ClinVar Allele:

68273

ClinVar RCV:

RCV000577614

ClinVar Variation:

53605

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Gln98Pro	CA326983 NM_000492.4:c.293A>C