Allele Registry

Canonical Allele Identifier: PA326949

Gene: CFTR HGNC NCBI

ClinVar RCV:

RCV000577587

RCV001509327

ClinVar Variation:

53582

HGVS (amino-acid)	Matching Registered Transcripts
NP_000483.3:p.His954Pro	CA326948 NM_000492.4:c.2861A>C