Canonical Allele Identifier: PA1139681117
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 990535
ClinVar RCV Id: RCV001278579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Val440Leu
CA368981953
NM_000492.4:c.1318G>C