Canonical Allele Identifier: PA2580116604
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1767226
ClinVar RCV Id: RCV002374187
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Val317Gly
CA368978446
NM_000492.4:c.950T>G