Canonical Allele Identifier: PA2741818497
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2567869
ClinVar RCV Id: RCV003311482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Pro41Arg
CA368987287
NM_000492.4:c.122C>G