Canonical Allele Identifier: PA2826369627
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1682835
ClinVar RCV Id: RCV002237740
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242975.1:p.Ala52Thr
CA9351975
NM_001256046.3:c.154G>A