Canonical Allele Identifier: PA2825194674
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 3231877
ClinVar RCV Id: RCV004518592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gln1038Arg
CA368990809
NM_000492.4:c.3113A>G