Canonical Allele Identifier: PA2825353498
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1335335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026896.3:p.Pro72Ser
CA405143263
NM_001031726.4:c.214C>T