ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2826369724
Gene: C19orf12
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1335335
ClinVar RCV Id:
RCV001816235
RCV002236177
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001242976.1:p.Pro72Ser
CA405143263
NM_001256047.2:c.214C>T