Canonical Allele Identifier: PA2499232873
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1043097
ClinVar RCV Id: RCV001347155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ala1256Gly
CA368974691
NM_000492.4:c.3767C>G