Canonical Allele Identifier: PA2825195462
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 3231911
ClinVar RCV Id: RCV004518626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ile1416Thr
CA368984375
NM_000492.4:c.4247T>C