Canonical Allele Identifier: PA2499232890
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1163871

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly921Val
CA368986685
NM_000492.4:c.2762G>T