Canonical Allele Identifier: PA2830059842
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 128538
ClinVar RCV Id: RCV000116508 RCV000356548 RCV000460848 RCV001847678
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_113636.2:p.Lys131Thr
CA152062
NM_031448.6:c.392A>C