Canonical Allele Identifier: PA645405886
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 411115
ClinVar RCV Id: RCV000476211 RCV001833592
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Tyr1381Cys
CA16612027
NM_000492.4:c.4142A>G