Canonical Allele Identifier: PA1139683046
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 861403
ClinVar RCV Id: RCV001067922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Lys1165Thr
CA368996057
NM_000492.4:c.3494A>C