Canonical Allele Identifier: PA915957526
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 824764
ClinVar RCV Id: RCV001247338 RCV001827204 RCV002261252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asn1432Lys
CA4451688
NM_000492.4:c.4296C>G
CA368984665
NM_000492.4:c.4296C>A