Canonical Allele Identifier: PA118640
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 7105
ClinVar RCV Id: RCV000007523 RCV000007524 RCV000058929 RCV000119038 RCV000626692 RCV000626693 RCV001004459 RCV001642198 RCV001831519 RCV002251888 RCV001787370 RCV001787371 RCV002243627 RCV003444054 RCV002490332 RCV003227599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Phe508del
CA118639
NM_000492.4:c.1521_1523del
CA164967779
NM_000492.4:c.1522_1524del