Canonical Allele Identifier: PA913194135
Gene: CFTR HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Tyr563His
CA368977018
NM_000492.4:c.1687T>C