Canonical Allele Identifier: PA658659890
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 455764
ClinVar RCV Id: RCV000551478
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Thr604Pro
CA368978040
NM_000492.4:c.1810A>C