Canonical Allele Identifier: PA2826674530
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_001269859.1:p.Thr38Met
CA9351891
NM_001282930.3:c.113C>T