Canonical Allele Identifier: PA326857
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53519
ClinVar RCV Id: RCV000577551
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Phe87Ile
CA326856
NM_000492.4:c.259T>A