Canonical Allele Identifier: PA326633
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53359
ClinVar RCV Id: RCV000577818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Pro574Ser
CA326632
NM_000492.4:c.1720C>T