Canonical Allele Identifier: PA658703899
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 495908
ClinVar RCV Id: RCV000586306 RCV001363162 RCV001835858
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ser776Leu
CA368980985
NM_000492.4:c.2327C>T