Canonical Allele Identifier: PA204144
Gene: CTRL HGNC NCBI

Linked Data

ClinVar Variation Id: 207886
ClinVar RCV Id: RCV000190171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001898.1:p.Ala73Thr
CA204143
NM_001907.3:c.217G>A