Canonical Allele Identifier: PA327628
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 54042
ClinVar RCV Id: RCV000577019 RCV002281557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gln237Glu
CA327627
NM_000492.4:c.709C>G