Canonical Allele Identifier: PA915957256
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 634830
ClinVar RCV Id: RCV000785631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ala1004_Ala1006del
CA913189832
NM_000492.4:c.3011_3019del