Canonical Allele Identifier: PA327047
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Thr1036Asn
CA327046
NM_000492.4:c.3107C>A