Allele Registry

Canonical Allele Identifier: PA327690

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV000577202

ClinVar Variation:

54084

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Phe305Val	CA327689 NM_000492.4:c.913T>G