Canonical Allele Identifier: PA326361
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53160

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Arg334Leu
CA326360
NM_000492.4:c.1001G>T