Canonical Allele Identifier: PA2580116000
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2023689
ClinVar RCV Id: RCV002875913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asp44Val
CA4450645
NM_000492.4:c.131A>T