ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825353579
Gene: C19orf12
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
40304
ClinVar RCV:
RCV000024323
ClinVar Variation:
31626
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001026896.3:p.Leu121Gln
CA260038
NM_001031726.4:c.362T>A