Canonical Allele Identifier: PA152063
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 128538
ClinVar RCV Id: RCV000116508 RCV000356548 RCV000460848 RCV001847678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242976.1:p.Lys131Thr
CA152062
NM_001256047.2:c.392A>C