ClinGen Allele Registry
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Canonical Allele Identifier:
PA916014071
Gene: C19orf12
HGNC
NCBI
Linked Data
ClinVar Variation Id:
31158
ClinVar RCV Id:
RCV000024154
RCV000415210
RCV000553096
RCV000509226
RCV001083182
RCV000714889
RCV001844017
RCV001847623
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001269860.1:p.Lys67Glu
CA259994
NM_001282931.3:c.199A>G