Canonical Allele Identifier: PA2741818501
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2567868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly85Arg
CA368972279
NM_000492.4:c.253G>A
CA368972281
NM_000492.4:c.253G>C