Canonical Allele Identifier: PA2499232868
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1053721
ClinVar RCV Id: RCV001362100 RCV001826016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Arg170Ser
CA4450747
NM_000492.4:c.508C>A