Canonical Allele Identifier: PA658703339
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 495893
ClinVar Variation Id: 2988284
ClinVar RCV Id: RCV003844467

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly404Arg
CA4450954
NM_000492.4:c.1210G>C
CA368981266
NM_000492.4:c.1210G>A