Canonical Allele Identifier: PA1139683384
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 918085
ClinVar RCV Id: RCV001175408 RCV002355138
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Phe1286Cys
CA368975550
NM_000492.4:c.3857T>G