Canonical Allele Identifier: PA2580121655
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2453661
ClinVar RCV Id: RCV003187796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Tyr1381Ser
CA4451652
NM_000492.4:c.4142A>C