Canonical Allele Identifier: PA2830059732
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 891192
ClinVar RCV Id: RCV001126323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_113636.2:p.Met38Thr
CA405145465
NM_031448.6:c.113T>C