Canonical Allele Identifier: PA658827185
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 557120

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Met82Val
CA368972258
NM_000492.4:c.244A>G