ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2825353434
Gene: C19orf12
HGNC
NCBI
Linked Data
ClinVar Variation Id:
402183
ClinVar RCV Id:
RCV000454138
RCV000486662
RCV001095481
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001026896.3:p.Gly54Val
CA9351930
NM_001031726.4:c.161G>T