Canonical Allele Identifier: PA658702769
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 495928
ClinVar RCV Id: RCV000630460 RCV001002302 RCV001508582 RCV002255467 RCV002491166 RCV004530642 RCV003471941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Val11Ile
CA4450601
NM_000492.4:c.31G>A