Canonical Allele Identifier: PA2499232893
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1163874

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Lys946Ile
CA368987171
NM_000492.4:c.2837A>T