Canonical Allele Identifier: PA326936
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53573
ClinVar RCV Id: RCV002433535
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.His939Arg
CA326935
NM_000492.4:c.2816A>G