Canonical Allele Identifier: PA327161
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53728
ClinVar RCV Id: RCV000577000 RCV001804780 RCV002483056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Glu1124del
CA327160
NM_000492.4:c.3371_3373del
CA368993254
NM_000492.4:c.3370G>T