Canonical Allele Identifier: PA327583
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 54013
ClinVar RCV Id: RCV000577168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Trp19Cys
CA327582
NM_000492.4:c.57G>T
CA368986811
NM_000492.4:c.57G>C