Allele Registry

Canonical Allele Identifier: PA326705

Gene: CFTR HGNC NCBI

Linked Data

ClinVar RCV:

RCV000046498

RCV000506455

RCV000763577

RCV001004277

RCV001009381

RCV001588828

RCV002228058

RCV002256004

RCV003473129

ClinVar Variation:

35833

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Gly622Asp	CA326704 NM_000492.4:c.1865G>A