Canonical Allele Identifier: PA2580116786
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1705987
ClinVar RCV Id: RCV002284517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Leu428Val
CA368981640
NM_000492.4:c.1282C>G