Canonical Allele Identifier: PA2825194601
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 3231874
ClinVar RCV Id: RCV004518589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asp984Gly
CA368989108
NM_000492.4:c.2951A>G