Canonical Allele Identifier: PA2580116574
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1765863
ClinVar RCV Id: RCV002378692

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Tyr304Ser
CA368978114
NM_000492.4:c.911A>C