Canonical Allele Identifier: PA2580116027
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1796028
ClinVar RCV Id: RCV002441402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Val93Asp
CA368974193
NM_000492.4:c.278T>A