Canonical Allele Identifier: PA2580118874
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1789454
ClinVar RCV Id: RCV002446459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Asn771Ser
CA368980951
NM_000492.4:c.2312A>G