Canonical Allele Identifier: PA2826369635
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1682830
ClinVar RCV Id: RCV002237736
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242975.1:p.Val57Leu
CA405143571
NM_001256046.3:c.169G>C