Canonical Allele Identifier: PA2580119815
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1809553
ClinVar RCV Id: RCV002481132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly1003Arg
CA368990351
NM_000492.4:c.3007G>A
CA368990353
NM_000492.4:c.3007G>C