Canonical Allele Identifier: PA326492
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53258
ClinVar RCV Id: RCV000666426 RCV003317059
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Ser485Cys
CA326491
NM_000492.4:c.1453A>T