Canonical Allele Identifier: PA327482
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2680711
ClinVar RCV Id: RCV003475690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Leu145His
CA327481
NM_000492.4:c.434T>A