Canonical Allele Identifier: PA658827274
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 554320
ClinVar RCV Id: RCV000669933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Met1137Thr
CA4451456
NM_000492.4:c.3410T>C