Canonical Allele Identifier: PA326924
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53565

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asp924Asn
CA326923
NM_000492.4:c.2770G>A