Canonical Allele Identifier: PA658703915
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 495910
ClinVar RCV Id: RCV000588117 RCV001834842 RCV001853982
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Leu802Phe
CA368981156
NM_000492.4:c.2406G>C
CA368981157
NM_000492.4:c.2406G>T