Canonical Allele Identifier: PA2580119284
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1697071
ClinVar RCV Id: RCV002267417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Thr908Ser
CA368986508
NM_000492.4:c.2722A>T
CA368986509
NM_000492.4:c.2723C>G