Canonical Allele Identifier: PA2830059841
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 31158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_113636.2:p.Lys131Glu
CA259994
NM_031448.6:c.391A>G