Canonical Allele Identifier: PA094281
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 7207

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.His949Tyr
CA325595
NM_000492.4:c.2845C>T