Canonical Allele Identifier: PA2825192954
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 3231940
ClinVar RCV Id: RCV004518655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Leu327Pro
CA368978608
NM_000492.4:c.980T>C