Canonical Allele Identifier: PA259995
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 31158
ClinVar RCV Id: RCV000024154 RCV000415210 RCV000553096 RCV000509226 RCV001083182 RCV000714889 RCV001844017 RCV001847623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242976.1:p.Lys131Glu
CA259994
NM_001256047.2:c.391A>G