Canonical Allele Identifier: PA325709
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 35878
ClinVar RCV Id: RCV000029533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly1298Ala
CA325708
NM_000492.4:c.3893G>C