Canonical Allele Identifier: PA658704204
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 495930
ClinVar RCV Id: RCV000588214 RCV000779527 RCV001293419 RCV001829623 RCV002476275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Tyr1092His
CA4451415
NM_000492.4:c.3274T>C