Canonical Allele Identifier: PA2573170359
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1502978
ClinVar RCV Id: RCV002022605
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Phe17Leu
CA368981378
NM_000492.4:c.49T>C
CA368981394
NM_000492.4:c.51C>A
CA368981397
NM_000492.4:c.51C>G