Canonical Allele Identifier: PA274057
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 188863
ClinVar RCV Id: RCV000169215 RCV001812146
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ile507Val
CA274056
NM_000492.4:c.1519A>G