Canonical Allele Identifier: PA658827184
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 549932
ClinVar RCV Id: RCV000664513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Glu56Gly
CA368972108
NM_000492.4:c.167A>G