Allele Registry

Canonical Allele Identifier: PA2826674550

Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000024154

RCV000415210

RCV000509226

RCV000553096

RCV000714889

RCV001083182

RCV001844017

RCV001847623

ClinVar Variation:

31158

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269859.1:p.Lys67Glu	CA259994 NM_001282930.3:c.199A>G