Canonical Allele Identifier: PA2826369637
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 579842
ClinVar RCV Id: RCV000703222
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242975.1:p.Val57Ala
CA9351924
NM_001256046.3:c.170T>C