Canonical Allele Identifier: PA915956323
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 819008
ClinVar RCV Id: RCV002319140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ala46Thr
CA368987369
NM_000492.4:c.136G>A