Canonical Allele Identifier: PA327017
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53630
ClinVar RCV Id: RCV000577813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Val1008Asp
CA327016
NM_000492.4:c.3023T>A