Canonical Allele Identifier: PA200679
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 193592
ClinVar RCV Id: RCV000173697 RCV000224343 RCV000366455 RCV001095146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asn417Lys
CA200678
NM_000492.4:c.1251C>A
CA368981481
NM_000492.4:c.1251C>G