Canonical Allele Identifier: PA2741814477
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2587615
ClinVar RCV Id: RCV003360969
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Phe316Ser
CA164953556
NM_000492.4:c.947T>C