Canonical Allele Identifier: PA2573069289
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1335335

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269860.1:p.Pro8Ser
CA405143263
NM_001282931.3:c.22C>T