Canonical Allele Identifier: PA658659776
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 455760
ClinVar RCV Id: RCV000542240 RCV001834713 RCV003317258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly404Val
CA368981275
NM_000492.4:c.1211G>T