Canonical Allele Identifier: PA326875
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53533
ClinVar RCV Id: RCV000577561

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Leu88Ser
CA326874
NM_000492.4:c.263T>C