Allele Registry

Canonical Allele Identifier: PA2826369708

Gene: C19orf12 HGNC NCBI

ClinVar Variation Id: 402183

HGVS (amino-acid)	Matching Registered Transcripts
NP_001242976.1:p.Gly54Val	CA9351930 NM_001256047.2:c.161G>T