Canonical Allele Identifier: PA2580116017
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2447394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Lys64Glu
CA368972149
NM_000492.4:c.190A>G