Allele Registry

Canonical Allele Identifier: PA326959

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV000673430

RCV002247434

RCV003476942

ClinVar Variation:

53589

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.Gly970Ser	CA326958 NM_000492.4:c.2908G>A