Canonical Allele Identifier: PA916014071
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 31158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269860.1:p.Lys67Glu
CA259994
NM_001282931.3:c.199A>G