Canonical Allele Identifier: PA326614
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 3063857
ClinVar RCV Id: RCV003988445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ala566Thr
CA326613
NM_000492.4:c.1696G>A