Canonical Allele Identifier: PA260221
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 35847
ClinVar RCV Id: RCV000029502 RCV001826513
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly921Glu
CA260220
NM_000492.4:c.2762G>A