Canonical Allele Identifier: PA645510215
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 439076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Met1140Ile
CA368993516
NM_000492.4:c.3420G>A
CA368993518
NM_000492.4:c.3420G>T
CA368993520
NM_000492.4:c.3420G>C