Canonical Allele Identifier: PA658659711
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 455782
ClinVar RCV Id: RCV000526413 RCV000590353 RCV001829535 RCV003338646 RCV002481755 RCV003235272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Arg170Cys
CA4450746
NM_000492.4:c.508C>T