Canonical Allele Identifier: PA2826369655
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 2579684
ClinVar RCV Id: RCV003328134 RCV003581925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242975.1:p.Pro82Thr
CA9351903
NM_001256046.3:c.244C>A