Allele Registry

Canonical Allele Identifier: PA260039

Gene: C19orf12 HGNC NCBI

ClinVar Allele:

40304

ClinVar RCV:

RCV000024323

ClinVar Variation:

31626

HGVS (amino-acid)	Matching Registered Transcripts
NP_001242976.1:p.Leu121Gln	CA260038 NM_001256047.2:c.362T>A