Canonical Allele Identifier: PA2580119667
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2498346
ClinVar RCV Id: RCV003222555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Lys951Glu
CA4451299
NM_000492.4:c.2851A>G