Canonical Allele Identifier: PA658827183
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 554829

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Arg31His
CA4450633
NM_000492.4:c.92G>A