Canonical Allele Identifier: PA658827213
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 553569
ClinVar RCV Id: RCV000669047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly451Val
CA368982277
NM_000492.4:c.1352G>T