Allele Registry

Canonical Allele Identifier: PA2825353579

Gene: C19orf12 HGNC NCBI

ClinVar RCV:

RCV000024323

ClinVar Variation:

31626

HGVS (amino-acid)	Matching Registered Transcripts
NP_001026896.3:p.Leu121Gln	CA260038 NM_001031726.4:c.362T>A