Canonical Allele Identifier: PA325692
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 35824
ClinVar RCV Id: RCV000029477 RCV000727666 RCV001004225 RCV002284179 RCV003473126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Pro5Leu
CA325691
NM_000492.4:c.14C>T