Canonical Allele Identifier: PA658803797
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 502578
ClinVar RCV Id: RCV000596788 RCV003493680 RCV002368030 RCV003317297
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Lys411Glu
CA4450960
NM_000492.4:c.1231A>G