Canonical Allele Identifier: PA2580118986
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1790586
ClinVar RCV Id: RCV002459587
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Pro798Arg
CA368981116
NM_000492.4:c.2393C>G