Canonical Allele Identifier: PA2825194519
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 3231868
ClinVar RCV Id: RCV004518583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Pro936Arg
CA368986971
NM_000492.4:c.2807C>G