Canonical Allele Identifier: PA2826369742
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1682823
ClinVar RCV Id: RCV002237729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242976.1:p.Thr102Met
CA9351891
NM_001256047.2:c.305C>T