Canonical Allele Identifier: PA2825353597
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1682819
ClinVar RCV Id: RCV002239974
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001026896.3:p.Arg134Gln
CA9351867
NM_001031726.4:c.401G>A