Canonical Allele Identifier: PA2825353593
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 31158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026896.3:p.Lys131Glu
CA259994
NM_001031726.4:c.391A>G