Allele Registry

Canonical Allele Identifier: PA326980

Gene: CFTR HGNC NCBI

ClinVar Allele:

68271

ClinVar RCV:

RCV000577309

RCV001009520

ClinVar Variation:

53603

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Asp979Val	CA326979 NM_000492.4:c.2936A>T