Canonical Allele Identifier: PA2580119769
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1797931
ClinVar RCV Id: RCV002440181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ala981Glu
CA368989072
NM_000492.4:c.2942C>A