Canonical Allele Identifier: PA186056
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 183298
ClinVar RCV Id: RCV000162119 RCV000292174 RCV000516097 RCV001231447 RCV003479030
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242976.1:p.Gly42Arg
CA186055
NM_001256047.2:c.124G>A
CA405145441
NM_001256047.2:c.124G>C