Allele Registry

Canonical Allele Identifier: PA2826369649

Gene: C19orf12 HGNC NCBI

ClinVar RCV:

RCV000211114

ClinVar Variation:

225875

HGVS (amino-acid)	Matching Registered Transcripts
NP_001242975.1:p.Pro72Leu	CA9351912 NM_001256046.3:c.215C>T