Canonical Allele Identifier: PA658659927
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 455766
ClinVar RCV Id: RCV000541753 RCV000781226 RCV002490942 RCV003736803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly817Val
CA4451183
NM_000492.4:c.2450G>T