Canonical Allele Identifier: PA2580120068
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1706008
ClinVar RCV Id: RCV002284538

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Leu1034Pro
CA368990785
NM_000492.4:c.3101T>C