Canonical Allele Identifier: PA913194287
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 632761
ClinVar RCV Id: RCV000780161
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ile1193Val
CA368996473
NM_000492.4:c.3577A>G