Canonical Allele Identifier: PA2830059771
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1335335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_113636.2:p.Pro72Ser
CA405143263
NM_031448.6:c.214C>T