Canonical Allele Identifier: PA2499232871
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1163870

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ala872Thr
CA368984080
NM_000492.4:c.2614G>A