Canonical Allele Identifier: PA2499232911
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1042311
ClinVar RCV Id: RCV001346243 RCV001825926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Thr599Ser
CA4451098
NM_000492.4:c.1796C>G
CA368977904
NM_000492.4:c.1795A>T