Allele Registry

Canonical Allele Identifier: PA916014070

Gene: C19orf12 HGNC NCBI

ClinVar Allele:

40304

ClinVar RCV:

RCV000024323

ClinVar Variation:

31626

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269860.1:p.Leu57Gln	CA260038 NM_001282931.3:c.170T>A