Canonical Allele Identifier: PA2573170402
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1440786
ClinVar RCV Id: RCV001967753

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ile86Asn
CA368972285
NM_000492.4:c.257T>A