Canonical Allele Identifier: PA2580118065
Gene: CFTR HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly673Arg
CA368979251
NM_000492.4:c.2017G>A
CA368979254
NM_000492.4:c.2017G>C